Surgiquip, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Surgiquip, Inc. makes
Surgiquip, Inc. manufactures powered surgical instruments for orthopedic and trauma procedures, including oscillating saws, bone reamers, sternum saws, drills, and reciprocating saws designed for precise bone cutting and preparation.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Snap Oscillating Saw Ref K931769
Regimes: 510(k) Registry: 510(k)Snap Bone Reamer Ref K935322
Regimes: 510(k) Registry: 510(k)Snap Sternum Saw Ref K935517
Regimes: 510(k) Registry: 510(k)Snap Drill Ref K935516
Regimes: 510(k) Registry: 510(k)Snap Reciprocating Saw Ref K935357
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgiquip, Inc. have in the registry?
The registry currently lists 5 devices for Surgiquip, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgiquip, Inc.'s devices?
Among its 5 most recently registered devices, Surgiquip, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Surgiquip, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Surgiquip, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Surgiquip, Inc. in the registry?
The most recently registered devices listed for Surgiquip, Inc. include SNAP OSCILLATING SAW, SNAP BONE REAMER, SNAP STERNUM SAW and SNAP DRILL.