Endomedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Endomedics, Inc. makes
Endomedics, Inc. manufactures orthopedic hip replacement components, including self-aligning acetabular implants, femoral stems, acetabular resurfacing components, and femoral resurfacing components designed for total hip arthroplasty procedures.
The company’s portfolio includes devices classified as Class II and Class III under FDA regulations, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Self-Aligning Acetabular Component Ref K831792
Regimes: 510(k) Registry: 510(k)New Jersey Femoral Stem Ref K842234
Regimes: 510(k) Registry: 510(k)New Jersey Acetabular Component & Ref K842202
Regimes: 510(k) Registry: 510(k)New Jersey Femoral Resurfacing Component Ref K842233
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endomedics, Inc. have in the registry?
The registry currently lists 4 devices for Endomedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endomedics, Inc.'s devices?
Among its 4 most recently registered devices, Endomedics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Endomedics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Endomedics, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Endomedics, Inc. in the registry?
The most recently registered devices listed for Endomedics, Inc. include SELF-ALIGNING ACETABULAR COMPONENT, NEW JERSEY FEMORAL STEM, NEW JERSEY ACETABULAR COMPONENT & and NEW JERSEY FEMORAL RESURFACING COMPONENT.