Cypress Medical Mfg., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cypress Medical Mfg., Inc. makes
Cypress Medical Mfg., Inc. manufactures orthopedic fixation devices, including bone screws and plates designed for internal skeletal stabilization, as well as cannulated bone screws for use in orthopedic surgeries.
The company’s products are regulated as Class II medical devices in the U.S. and are listed under the FDA’s 510(k) clearance pathway. These devices are intended for surgical applications requiring rigid fixation of bone fragments.
Catalogue
Cypress Medical Bone Screw & Plates Ref K894719
Regimes: 510(k) Registry: 510(k)Cypress Cannulated Bone Screw Ref K894830
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cypress Medical Mfg., Inc. have in the registry?
The registry currently lists 2 devices for Cypress Medical Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cypress Medical Mfg., Inc.'s devices?
Among its 2 most recently registered devices, Cypress Medical Mfg., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cypress Medical Mfg., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cypress Medical Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cypress Medical Mfg., Inc. in the registry?
The most recently registered devices listed for Cypress Medical Mfg., Inc. include CYPRESS MEDICAL BONE SCREW & PLATES and CYPRESS CANNULATED BONE SCREW.