Geneva (July 30, 2025) – SGS, the world’s leading testing, inspection and certification company, has published SafeGuardS 107.25, summarizing the EU’s changes to its Persistent Organic Pollutants (POP) Recast Regulation, regarding perfluorooctanoic acid (PFOA), its salts and PFOA-related compounds.

These chemicals are used for their fire- and water-resistant properties. However, due to their persistence in the environment and potential health risks, safer alternatives are increasingly being sought.

 

The EU issued Commission Delegated Regulation (EU) 2025/1399 on July 14, 2025, amending the entry for PFOA, its salts and PFOA-related compounds under Part A to Annex 1 of Regulation 2019/1021 of the POP Recast Regulation. The amendment takes effect on August 3, 2025.

 

SGS experts publish SafeGuardS to keep stakeholders informed about regulatory changes that could impact their business. SafeGuardS 107.25 provides further information on the relevant entry in Commission Delegated Regulation (EU) 2025/1399, and a link to the official text.

 

Stakeholders are encouraged to refer to the original SafeGuardS 107.25 for more details.

 

SGS chemical testing services
SGS offers a comprehensive range of testing services to help manufacturers and suppliers ensure their products are safe and comply with national and international regulations concerning harmful chemicals. In the end, it’s only trusted because it’s tested. Learn more about SGS’s chemical testing services.

 

SGS SafeGuardS keep you up to date with the latest news and developments in the consumer goods industry. Read the full EU Revises Entry for PFOA and PFOA-related Compounds under POP Recast Regulation SafeGuardS.

 

Subscribe today and receive SGS SafeGuardS direct to your inbox.

 

For further information contact:

 

Dr. HingWo Tsang
Global Information and Innovation Manager
Tel: +852 2774 7420
Website: www.sgs.com/hardlines
LinkedIn: SGS Connectivity & Products

 

About SGS
SGS is the world’s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries, supported by a team of 99,500 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance and sustainability.

 

Our brand promise – when you need to be sure – underscores our commitment to trust, integrity and reliability, enabling businesses to thrive with confidence. We proudly deliver our expert services through the SGS name and trusted specialized brands, including Brightsight, Bluesign, Maine Pointe and Nutrasource.

 

SGS is publicly traded on the SIX Swiss Exchange under the ticker symbol SGSN (ISIN CH1256740924, Reuters SGSN.S, Bloomberg SGSN:SW).

FORTSON, GA — TiNives Original, LLC has officially released two new knife lines—the Covert Series and the 3.65 Ultralite Flipper—marking a major milestone in the brand’s relaunch following its return to the knife-making scene in 2021. Known for their highly engineered folding knives from the late 1990s, TiNives continues to push mechanical and aesthetic boundaries with American-made tools crafted for both performance and collectibility.

A Legacy of Innovation

 

TiNives was originally founded in 1997 by Scott Self, gaining recognition in the knife world for introducing the “Zero Play Knife”, a highly complex folder with over 100 components and a button-activated locking mechanism. The company paused production in the mid-2000s, but in 2021 Self partnered with longtime collaborator Larry Chew to revive the brand with a renewed focus on precision CNC machining and fine metalwork.

Today, TiNives operates out of a 15,000-square-foot facility in Fortson, Georgia, combining modern machining with handcrafted finishing. The production team includes Scott Self, Larry Chew, and Jason Potts, each contributing to the company's focus on building knives that are both functional and visually distinctive.

The Covert Series: Built for Speed and Style

 

The Covert Series introduces a new generation of double-action automatic knives, all featuring Larry Chew’s Covert button lock-out mechanism and smooth, responsive action powered by ceramic bearings and a ceramic detent ball.

Key specifications found across Covert models include:

 

  • Blade Length: 3.65 inches
  • Blade Materials: Options include CPM Magnacut and Nichols Intrepid pattern Damascus
  • Handle Materials: Titanium, carbon fiber, Timascus, and Damascus bolsters
  • Rockwell Hardness: Up to 63 HRC depending on the model
  • Overall Length: 8.125 inches
  • Weight: Varies by model, typically 3.6–4.0 ounces
  • Titanium Frames, Liners, and Hardware
  • Serial Numbered for Traceability

Each Covert model is assembled and finished in-house, reflecting the brand’s attention to detail and metal artistry.

The 3.65 Ultralite Flipper: Lightweight, Functional, American-Made

 

The 3.65 Ultralite Flipper, also designed by Larry Chew, is a manual folding knife focused on fast deployment and low-profile carry. It features:

  • Bead-Blasted Titanium Handles
  • 3.65" CPM Magnacut Blade (63–64 Rc)
  • Lightweight Carbon Fiber Backspacer
  • Ceramic Bearings and Detent Ball
  • Anodized Titanium Hardware and Pocket Clip
  • Open Length: 8.125 inches
  • Closed Length: 4.562 inches
  • Weight: 3.2 ounces
  • Serial Numbered

The Flipper is engineered for users who prioritize compact form, premium materials, and precision operation in a fully U.S.-made tool.

Available Now

 

All TiNives products are proudly designed, machined, and assembled in the USA. The latest models in both the Covert and Flipper lines are available now at www.tinivesoriginal.com, with select configurations featuring materials such as Timascus, Nichols Damascus, and titanium anodizing.

Media Contact:

TiNives Original, LLC

Phone: (762) 821-1478

Address: 1825 Smith Road Fortson, GA 31808

Email: This email address is being protected from spambots. You need JavaScript enabled to view it.

Website: https://www.tinivesoriginal.com

About TiNives Original

 

Founded in 1997 and reestablished in 2021, TiNives Original, LLC designs and produces precision-engineered folding knives in Fortson, Georgia. Known for its early innovations in button lock mechanisms and multi-component knife construction, the company now focuses on CNC-machined, American-made knives that blend mechanical innovation with detailed metal artistry.

Geneva (July 28, 2025) – SGS, the world’s leading testing, inspection and certification company, has published a Consumer Compact article on how new EU sustainability regulations are set to transform consumer product markets.

The Ecodesign for Sustainable Products Regulation (ESPR) and accompanying Digital Product Passport (DPP) are key elements of the EU Green Deal, supporting a shift to a more circular and climate-neutral economy. These measures will impact how products are designed, manufactured, marketed and disposed of – from fashion and furniture to electronics and toys.

ESPR introduces minimum requirements for durability, repairability and recyclability, while also banning the destruction of unsold goods in many categories. At the same time, the DPP will digitally track each product’s sustainability profile across its life cycle, improving transparency for consumers and accountability for brands.

The article outlines priority product groups targeted by the EU’s latest working plan, including textiles, furniture, mattresses and intermediate materials such as aluminum and steel. The implications for businesses are far-reaching, demanding action on material sourcing, supply chain traceability and digital data management.

With full rollout expected by 2027/28, forward-thinking brands can gain a competitive edge by aligning early with these regulatory shifts. The article also discusses the role of DPPs in related sectors, such as toy safety under the proposed Toy Safety Regulation.

Read the original Consumer Compact article, ‘How will the EU ESPR & DPP impact consumer product markets.’  

SGS solutions
SGS provides integrated sustainability services including DPP readiness assessments, ecodesign advisory, and digital compliance verification. Our IMPACT NOW for sustainability program supports brands in meeting EU regulatory requirements while building consumer trust. In the end, it’s trusted because it’s tested.

Learn more about SGS’s circular economy services

Subscribe to receive SGS Consumer Compact direct to your inbox.  

For more information, please contact:

Kelly Peng

Technical Team, Hardlines, Connectivity & Products
Tel: +86(0)755 2532 8242
Website: www.sgs.com/hardlines
LinkedIn: SGS Connectivity & Products

About SGS

SGS is the world’s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries, supported by a team of 99,500 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance and sustainability.

Our brand promise – when you need to be sure – underscores our commitment to trust, integrity and reliability, enabling businesses to thrive with confidence. We proudly deliver our expert services through the SGS name and trusted specialized brands, including Brightsight, Bluesign, Maine Pointe and Nutrasource.

SGS is publicly traded on the SIX Swiss Exchange under the ticker symbol SGSN (ISIN CH1256740924, Reuters SGSN.S, Bloomberg SGSN:SW).

 

Geneva (July 28, 2025) – SGS, the world’s leading testing, inspection and certification company, has published SafeGuardS 101.25 to inform stakeholders of important amendments to Minnesota’s law on products containing intentionally added per- and polyfluoroalkyl substances (PFAS).

 

Signed into law on June 14, 2025, SF 3 (Chapter 1) expands exemptions under Minnesota Statutes §116.943, originally introduced in HF 2310 (2023), which restricts PFAS in 11 product categories starting January 1, 2025. The amendments, effective immediately, provide critical clarifications and exemptions that support manufacturers and importers in meeting the state’s evolving environmental protection standards.

 

Key changes include:
- Exemption for PFAS in internal or electronic components: products containing intentionally added PFAS exclusively in electronic or internal components are now excluded from the 2025 prohibitions
- Exemption for certain children’s vehicles: off-highway vehicles, ATVs, off-highway motorcycles, snowmobiles and electric-assisted bicycles are no longer considered “juvenile products” under the regulation
- Updated definitions: ’internal components’ are defined as parts not designed to be touched during intended use, including battery housings

 

Additional requirements and deadlines remain in place:
- Disclosure requirement by January 1, 2026: for all products containing intentionally added PFAS
- Total ban by January 1, 2032: unless the commissioner determines the use of PFAS to be unavoidable

 

SGS publishes SafeGuardS to help stakeholders remain up to date on critical regulatory changes. SafeGuardS 101.25 provides detailed insights into Minnesota’s PFAS legislation and its expanded exemptions, enabling companies to plan for compliance and continued market access.

 

Stakeholders are encouraged to review SafeGuardS 101.25 for comprehensive guidance on navigating these regulatory updates.

 

SGS Chemical Testing
SGS offers a comprehensive range of testing services to help manufacturers and suppliers ensure their products are safe and comply with national and international regulations concerning harmful chemicals. In the end, it’s only trusted because it’s tested. Learn more about SGS chemical testing services.

 

SGS SafeGuardS keep you up to date with the latest news and developments in the consumer goods industry. Read the full Minnesota, USA, Revises Law on PFAS Ban in Products to Include Certain Exemptions SafeGuardS.

 

Subscribe today and receive SGS SafeGuardS direct to your inbox.

 

For further information contact:

 

Dr. Hingwo Tsang
Global Information and Innovation Manager
Tel: +852 2774 7420

 

Melanie Tamayo
Senior Technical Manager, SGS NA
Tel: +1 312 414 9394

 

Website: www.sgs.com/cp
LinkedIn: SGS Connectivity & Products

 

About SGS
SGS is the world’s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries, supported by a team of 99,500 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance and sustainability.

 

Our brand promise – when you need to be sure – underscores our commitment to trust, integrity and reliability, enabling businesses to thrive with confidence. We proudly deliver our expert services through the SGS name and trusted specialized brands, including Brightsight, Bluesign, Maine Pointe and Nutrasource.

 

SGS is publicly traded on the SIX Swiss Exchange under the ticker symbol SGSN (ISIN CH1256740924, Reuters SGSN.S, Bloomberg SGSN:SW).

Federal Trade Commission enforcement against medical spas has intensified dramatically, with recent cases producing judgments exceeding $6.6 million as regulators crack down on practices that fail to substantiate their advertising claims with competent scientific evidence. The aesthetic medicine industry is discovering that promotional strategies common in retail and hospitality sectors can trigger federal investigations when applied to medical treatments.

The FTC's healthcare advertising standards require the same level of scientific substantiation typically reserved for pharmaceutical companies, creating compliance challenges for an industry built on visual marketing and client testimonials.


Treatment Guarantees Spark Federal Investigation

Medical spas nationwide are facing penalties up to $43,792 per violation for making treatment promises that cannot be scientifically supported. Common triggers include advertising procedures as completely pain-free, promising permanent results from treatments that provide temporary benefits, or guaranteeing specific aesthetic outcomes that vary significantly between patients.

The enforcement pattern reveals that federal regulators view even seemingly minor marketing exaggerations as serious violations. Claims about treatment comfort levels, duration of results, or universal effectiveness must be supported by reliable clinical evidence—not just practitioner experience or patient feedback.

Beyond individual violation penalties, the FTC can pursue disgorgement of profits and require complete consumer refunds, potentially reaching millions of dollars in total financial exposure. The agency also imposes ongoing restrictions on future advertising practices that can permanently limit how violating businesses promote their services.


Visual Marketing Under Federal Scrutiny

The before-and-after photograph violations represent a particularly complex area of FTC enforcement. Medical spas that steal images from other providers, digitally enhance results, or present exceptional outcomes as typical patient experiences face both advertising violations and potential fraud allegations.

One documented enforcement case involved a medical spa that faced $35,000 in penalties for using stolen before-and-after photos while simultaneously violating privacy regulations through improper website tracking. The case demonstrates how advertising violations often compound with other regulatory failures, multiplying potential penalties and legal exposure.

The FTC requires that visual marketing materials accurately represent typical patient outcomes and include appropriate disclaimers when results vary significantly. The agency has specifically targeted practices that present their best results as standard outcomes without acknowledging the range of possible patient experiences.


Influencer Marketing Creates Corporate Liability

The rise of social media marketing has created new areas of FTC enforcement that directly impact medical spa advertising strategies. When practices compensate influencers with money or free treatments, they become legally responsible for all claims made by those endorsers about the business and its services.

This corporate liability extends to unsubstantiated claims made by influencers about treatment effectiveness, safety, or superiority over competitors. The FTC has already warned over 90 social media influencers about required disclosure practices, signaling increased enforcement activity in this marketing channel.

Medical spas must now ensure that all compensated endorsers comply with federal truth-in-advertising requirements, creating vendor management responsibilities that many practices are unprepared to handle effectively.


Coordinated Federal Enforcement

The FTC works jointly with the Food and Drug Administration to identify and prosecute advertising violations, creating a coordinated federal response that increases compliance pressure on medical spas. Companies that receive cease-and-desist orders must respond within 15 days or face escalated enforcement actions with penalties similar to direct FTC violations.

This joint enforcement approach means that medical spas face simultaneous scrutiny from multiple federal agencies, each with different areas of expertise and enforcement authority. The coordinated response can result in overlapping investigations that examine both advertising practices and underlying treatment protocols.

“The federal enforcement landscape has fundamentally changed how medical spas need to approach their marketing,” said Lynn Wilkinson, CEO of BloomDigital, a digital marketing agency that helps growth-focused med spas attract more clients. “What worked five years ago can now trigger a federal investigation.”


Financial Impact Beyond Direct Penalties

The true cost of FTC enforcement extends far beyond direct violation penalties to include legal defense fees, business interruption losses, and reputation damage that can persist long after enforcement actions conclude.

Medical spas that face federal investigation often spend more on legal representation than the underlying penalties, while dealing with operational disruptions that affect patient care and staff retention. The enforcement actions also create insurance implications, as professional liability carriers may exclude coverage for advertising violations or increase premiums for practices with enforcement histories.

These secondary costs can exceed the direct penalties imposed by federal regulators.


Conclusion

Medical spas should implement comprehensive review processes for all advertising materials, ensure staff understand federal requirements for treatment claims, and establish clear protocols for working with social media influencers and other marketing partners. The cost of preventive compliance measures remains minimal compared to the financial exposure created by federal enforcement actions.

The FTC's increased focus on healthcare advertising represents a permanent shift in the regulatory environment facing medical spas. Practices that adapt their med spa marketing strategies to federal requirements can continue growing, while those that ignore these standards face existential business risks.

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