Levtech, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Levtech, Inc. makes
Levtech, Inc. manufactures orthopedic devices including the LEVTECH TITANIUM BONE WIRE, LEVTECH CLAMP APPLIER, HALIFAX SPINAL CLAMP, LEVTECH COMPOSITE TRACTION TONGS, and LEVTECH BONE SCREW.
The company's portfolio consists of Class I and Class II devices listed in the FDA 510(k) registry, and Levtech, Inc. is based in the US.
Catalogue
Levtech Titanium Bone Wire Ref K910128
Regimes: 510(k) Registry: 510(k)Levtech Clamp Applier Ref K874023
Regimes: 510(k) Registry: 510(k)Halifax Spinal Clamp Ref K850039
Regimes: 510(k) Registry: 510(k)Levtech Composite Traction Tongs Ref K873693
Regimes: 510(k) Registry: 510(k)Levtech Bone Screw Ref K901144
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Levtech, Inc. have in the registry?
The registry currently lists 5 devices for Levtech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Levtech, Inc.'s devices?
Among its 5 most recently registered devices, Levtech, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Levtech, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Levtech, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Levtech, Inc. in the registry?
The most recently registered devices listed for Levtech, Inc. include LEVTECH TITANIUM BONE WIRE, LEVTECH CLAMP APPLIER, HALIFAX SPINAL CLAMP and LEVTECH COMPOSITE TRACTION TONGS.