Medicinelodge, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mli Interference Screw Ref K953350
Regimes: 510(k) Registry: 510(k)Expanded Body Suture Ref K961025
Regimes: 510(k) Registry: 510(k)Mli Modular Staple Ref K962705
Regimes: 510(k) Registry: 510(k)Mli Soft Tissue Screw & Washer System Ref K962194
Regimes: 510(k) Registry: 510(k)Cross Pin Ref K961920
Regimes: 510(k) Registry: 510(k)Medicinelodge, Inc. Set Screw Ref K961905
Regimes: 510(k) Registry: 510(k)Zipknot, Model 1017-3000 Ref K072525
Regimes: 510(k) Registry: 510(k)Medicinelodge Zipknot Ref K051488
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medicinelodge, Inc. have in the registry?
The registry currently lists 8 devices for Medicinelodge, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medicinelodge, Inc.'s devices?
Among its 8 most recently registered devices, Medicinelodge, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Medicinelodge, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Medicinelodge, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medicinelodge, Inc. in the registry?
The most recently registered devices listed for Medicinelodge, Inc. include MLI INTERFERENCE SCREW, EXPANDED BODY SUTURE, MLI MODULAR STAPLE and MLI SOFT TISSUE SCREW & WASHER SYSTEM.