Gynemetrics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Gynemetrics, Inc. makes
Gynemetrics, Inc. manufactures uterine sounds, cervical dilators, menstrual aspiration kits, and uterine curettes.
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
Uterine Sound Ref K802315
Regimes: 510(k) Registry: 510(k)Cervical Dilator Ref K811568
Regimes: 510(k) Registry: 510(k)Menstrual Aspiration Kits Ref K803210
Regimes: 510(k) Registry: 510(k)Uterine Curette Ref K802313
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gynemetrics, Inc. have in the registry?
The registry currently lists 4 devices for Gynemetrics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gynemetrics, Inc.'s devices?
Among its 4 most recently registered devices, Gynemetrics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Gynemetrics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Gynemetrics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gynemetrics, Inc. in the registry?
The most recently registered devices listed for Gynemetrics, Inc. include UTERINE SOUND, CERVICAL DILATOR, MENSTRUAL ASPIRATION KITS and UTERINE CURETTE.