Medifix, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Medifix, Inc. makes
Medifix, Inc. manufactures single and double puncture laparoscopes, ureteroscopes, and arthroscopes. These devices are designed for minimally invasive surgical procedures, including laparoscopic abdominal surgeries, ureteral interventions, and joint examinations. The laparoscopes facilitate endoscopic visualization of internal organs, while the ureteroscopes and arthroscopes enable targeted inspection and treatment of the urinary tract and joints, respectively.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for use within the United States, adhering to regulatory standards for surgical and diagnostic instruments. Medifix, Inc. is headquartered in the US.
Catalogue
Medifix Single And Double Puncture Laparoscopes Ref K992480
Regimes: 510(k) Registry: 510(k)Medifix Ureteroscope Ref K011325
Regimes: 510(k) Registry: 510(k)Medifix Inc. Ref K992483
Regimes: 510(k) Registry: 510(k)Arthroscope / Medifix Inc. Ref K992474
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medifix, Inc. have in the registry?
The registry currently lists 4 devices for Medifix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medifix, Inc.'s devices?
Among its 4 most recently registered devices, Medifix, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medifix, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medifix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medifix, Inc. in the registry?
The most recently registered devices listed for Medifix, Inc. include MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES, MEDIFIX URETEROSCOPE, MEDIFIX INC. and ARTHROSCOPE / MEDIFIX INC..