Protek, Inc.
United StatesFDA applicant, unverified
- Devices
- 25
What Protek, Inc. makes
Protek, Inc. makes orthopedic implants, including acetabular cups, femoral heads, hip prostheses, knee prostheses, and wrist prostheses. Their products include cementless and cemented fixation devices, as well as modular and fixed components. They also produce staples and various alloy materials for use in their devices.
The company's portfolio is regulated as Class II and Class III devices and is listed in the FDA 510(k) registry. Protek, Inc. is based in the US.
Catalogue
Search and filter all 25 devicesFrequently asked questions
How many devices does Protek, Inc. have in the registry?
The registry currently lists 25 devices for Protek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Protek, Inc.'s devices?
Among its 25 most recently registered devices, Protek, Inc. has devices listed in FDA 510(k) (25 devices).
What risk classes do Protek, Inc.'s devices fall under?
Among its 25 most recently registered devices, the classes recorded for Protek, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Protek, Inc. in the registry?
The most recently registered devices listed for Protek, Inc. include CLX ACETABULAR CUP (WAGNER) FOR CEMENTLESS FIXAT., SAMUELSON ACETABULAR CUP, FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR and DAY STAPLE.