Medcanica, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Medcanica, Inc. makes
Medcanica, Inc. manufactures orthopedic fixation devices, including the ULTRA-CBX for bone stabilization, the METACARPAL and PHALANGEAL FIXATION SYSTEMS for hand and finger fractures, and specialized ports like the INTERCOSTAL LOCKABLE-DIRECTABLE PORT for surgical access. The company also produces an INSTRUMENT DAMPING PORT designed to reduce noise during procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Medcanica, Inc. is based in the United States.
Catalogue
Ultra-Cbx Ref K991486
Regimes: 510(k) Registry: 510(k)Metacarpal Fixation System Ref K991064
Regimes: 510(k) Registry: 510(k)Instrument Damping Port Ref K011373
Regimes: 510(k) Registry: 510(k)Phalangeal Fixation System Ref K994232
Regimes: 510(k) Registry: 510(k)Intercostal Lockable-Directable Port Ref K011349
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medcanica, Inc. have in the registry?
The registry currently lists 5 devices for Medcanica, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medcanica, Inc.'s devices?
Among its 5 most recently registered devices, Medcanica, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medcanica, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medcanica, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medcanica, Inc. in the registry?
The most recently registered devices listed for Medcanica, Inc. include ULTRA-CBX, METACARPAL FIXATION SYSTEM, INSTRUMENT DAMPING PORT and PHALANGEAL FIXATION SYSTEM.