D3 Dc, LLC /Stabilynx, Inc.
Country not established
- Devices
- 1
What D3 Dc, LLC /Stabilynx, Inc. makes
D3 Dc, LLC / Stabilynx, Inc. manufactures the Stabilynx PEEK Suture Anchor, a bioinert, resorbable-free orthopedic fixation device designed for soft tissue and ligament reattachment in joint surgeries, such as rotator cuff repairs and ACL reconstructions.
The Stabilynx PEEK Suture Anchor is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is headquartered in the United States.
Catalogue
Stabilynx PEEK Suture Anchor Ref K142643
510(k) 510(k)
Frequently asked questions
How many devices does D3 Dc, LLC /Stabilynx, Inc. have in the registry?
The registry currently lists 1 device for D3 Dc, LLC /Stabilynx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D3 Dc, LLC /Stabilynx, Inc.'s devices?
Among its 1 most recently registered device, D3 Dc, LLC /Stabilynx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do D3 Dc, LLC /Stabilynx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D3 Dc, LLC /Stabilynx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D3 Dc, LLC /Stabilynx, Inc. in the registry?
The most recently registered devices listed for D3 Dc, LLC /Stabilynx, Inc. include Stabilynx PEEK Suture Anchor.