Link America, Inc.
United StatesFDA applicant, unverified
- Devices
- 21
What Link America, Inc. makes
Link America, Inc. manufactures orthopedic fixation devices, including cortical screws, hip prostheses systems, ceramic femoral heads, radius osteotomy and plating systems, dynamic staples, spinal instrumentation (e.g., Harrington-type scoliosis systems), acetabular revision mesh cups, small bone plates, and external mini-fixator systems for limb alignment.
The company’s products are regulated under FDA Class I, II, and III classifications, with many authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Search and filter all 21 devicesFrequently asked questions
How many devices does Link America, Inc. have in the registry?
The registry currently lists 21 devices for Link America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Link America, Inc.'s devices?
Among its 21 most recently registered devices, Link America, Inc. has devices listed in FDA 510(k) (21 devices).
What risk classes do Link America, Inc.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Link America, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Link America, Inc. in the registry?
The most recently registered devices listed for Link America, Inc. include LINK CORTICAL SCREWS, LINK CONTOUR RIBBED HIP PROSTHESES SYSTEM, LINK CERAMIC HEADS 12/14 X 32MM and SCHWABE RADIUS PLATES.