Tribofilm Research, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tribofilm Research, Inc. makes
Tribofilm Research, Inc. manufactures lubricated, silicone-free syringes designed to reduce friction and improve ease of use, including the TRIBOGLIDE and StaClear syringe models. These products are intended for single-use medical injections and aim to enhance patient comfort during administration.
The company’s portfolio is classified under FDA’s Class II medical devices and is authorised through the 510(k) pathway. These devices are listed in the FDA’s regulatory database, and the company operates from the United States.
Catalogue
Triboglide Lubricated Silicone-Free Syringe Ref K071027
Regimes: 510(k) Registry: 510(k)StaClear Syringe Ref K200242
Regimes: CE MDR 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tribofilm Research, Inc. have in the registry?
The registry currently lists 2 devices for Tribofilm Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tribofilm Research, Inc.'s devices?
Among its 2 most recently registered devices, Tribofilm Research, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tribofilm Research, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tribofilm Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tribofilm Research, Inc. in the registry?
The most recently registered devices listed for Tribofilm Research, Inc. include TRIBOGLIDE LUBRICATED SILICONE-FREE SYRINGE and StaClear Syringe.