Medishield, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
What Medishield, Inc. makes
Medishield, Inc. makes a monomer evacuation system, microfenestrated hip replacement components, battery-powered mini-drills, ankle instruments (Freeman-Swanson), a Selectatec system, air-powered coldrills, and a Spectrascan device.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Monomer Evacuation System Ref K780202
Regimes: 510(k) Registry: 510(k)Microfenestrated Hip Replacement Compon. Ref K770161
Regimes: 510(k) Registry: 510(k)Hmd-2000 Battery-Powered Mini-Drill, The Ref K780645
Regimes: 510(k) Registry: 510(k)Ankle Instruments (Freeman-Swanson) Ref K761021
Regimes: 510(k) Registry: 510(k)Selectatec System Ref K760668
Regimes: 510(k) Registry: 510(k)Air-Pwoered Coldrill Ref K780646
Regimes: 510(k) Registry: 510(k)Ankle (Freeman-Swanson) Ref K761020
Regimes: 510(k) Registry: 510(k)Spectrascan Ref K781103
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medishield, Inc. have in the registry?
The registry currently lists 8 devices for Medishield, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medishield, Inc.'s devices?
Among its 8 most recently registered devices, Medishield, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Medishield, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Medishield, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medishield, Inc. in the registry?
The most recently registered devices listed for Medishield, Inc. include MONOMER EVACUATION SYSTEM, MICROFENESTRATED HIP REPLACEMENT COMPON., HMD-2000 BATTERY-POWERED MINI-DRILL, THE and ANKLE INSTRUMENTS (FREEMAN-SWANSON).