Nexmed, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Nexmed, Inc. makes
Nexmed, Inc. manufactures orthopedic implants, including femoral stems for hip replacements, modular total hip and knee systems, and cancellous bone screws designed for bone fixation. The NEXLOCK and NEXFLEX product lines provide modular components for hip and knee arthroplasty, while the cancellous bone screws are intended for internal fixation in bone surgery.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company’s products are listed in the FDA’s 510(k) database. Nexmed, Inc. is based in the United States.
Catalogue
Nexlock Femoral Stem Ref K955171
Regimes: 510(k) Registry: 510(k)Nexflex Total Hip System Ref K952629
Regimes: 510(k) Registry: 510(k)Nexflex Total Hip System Ref K033580
Regimes: 510(k) Registry: 510(k)Nexmed Cancellous Bone Screws Ref K951656
Regimes: 510(k) Registry: 510(k)Nexflex Femoral Stem, Standard Design Ref K955170
Regimes: 510(k) Registry: 510(k)Nexflex Total Knee System Ref K991882
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nexmed, Inc. have in the registry?
The registry currently lists 6 devices for Nexmed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nexmed, Inc.'s devices?
Among its 6 most recently registered devices, Nexmed, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Nexmed, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Nexmed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nexmed, Inc. in the registry?
The most recently registered devices listed for Nexmed, Inc. include NEXLOCK FEMORAL STEM, NEXFLEX TOTAL HIP SYSTEM, NEXMED CANCELLOUS BONE SCREWS and NEXFLEX FEMORAL STEM, STANDARD DESIGN.