Sur-Med Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Sur-Med Instruments, Inc. makes
Sur-Med Instruments, Inc. makes surgical retractors, tube inserters, and rongeurs, including the Kodner Anal Perioneal Retractor, T-Tube Inserter, and Special Rongeur.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Kodner Anal Perioneal Retractor Ref K870897
Regimes: 510(k) Registry: 510(k)T-Tube Inserter Ref K870978
Regimes: 510(k) Registry: 510(k)Special Rongeur Ref K903401
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sur-Med Instruments, Inc. have in the registry?
The registry currently lists 3 devices for Sur-Med Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sur-Med Instruments, Inc.'s devices?
Among its 3 most recently registered devices, Sur-Med Instruments, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sur-Med Instruments, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sur-Med Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sur-Med Instruments, Inc. in the registry?
The most recently registered devices listed for Sur-Med Instruments, Inc. include KODNER ANAL PERIONEAL RETRACTOR, T-TUBE INSERTER and SPECIAL RONGEUR.