Suturetech, Inc.
United Statesfrom the FDA registration address FDA FEI 3043861298
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
All-Suture Dual Anchor System Ref K250095
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043861298
- Address
- 810 Laurelwood Dr, Durham, NC, 27705
Frequently asked questions
How many devices does Suturetech, Inc. have in the registry?
The registry currently lists 2 devices for Suturetech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suturetech, Inc.'s devices?
Among its 2 most recently registered devices, Suturetech, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Suturetech, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Suturetech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Suturetech, Inc. in the registry?
The most recently registered devices listed for Suturetech, Inc. include RapidFix™ All-Suture Dual Anchor PKG-90-STK-100100 and All-Suture Dual Anchor System.