Retrax, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Retrax, Inc. makes
Retrax, Inc. manufactures the RETRAX Safety Syringe, a needle safety device designed to reduce occupational exposure to bloodborne pathogens by retracting the needle into the syringe body after use.
The RETRAX Safety Syringe is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Magnetic Point Guard For Surgical Needles Ref K920706
Regimes: 510(k) Registry: 510(k)Retrax Safety Syringe Ref K901508
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retrax, Inc. have in the registry?
The registry currently lists 2 devices for Retrax, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retrax, Inc.'s devices?
Among its 2 most recently registered devices, Retrax, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Retrax, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Retrax, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retrax, Inc. in the registry?
The most recently registered devices listed for Retrax, Inc. include MAGNETIC POINT GUARD FOR SURGICAL NEEDLES and RETRAX SAFETY SYRINGE.