Gynescope Corp.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Gynescope Laparoscopic Trocars And Sleeves Ref K902656
Regimes: 510(k) Registry: 510(k)Gynecological Instrumentation Ref K895225
Regimes: 510(k) Registry: 510(k)Gynescope Monopolar Forceps And Electrodes Ref K902658
Regimes: 510(k) Registry: 510(k)Ott Insufflation Filter Tubing Ref K900878
Regimes: 510(k) Registry: 510(k)Modified Metal Speculum & Special Bullet Forceps Ref K902019
Regimes: 510(k) Registry: 510(k)Wallace Intrauterine Insemination Catheter Ref K901530
Regimes: 510(k) Registry: 510(k)Croak Ovarian Biopsy Forcep Ref K902049
Regimes: 510(k) Registry: 510(k)Gynescope Laparoscopes Ref K902655
Regimes: 510(k) Registry: 510(k)Gynescope Laparoscopic Forceps Ref K902657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gynescope Corp. have in the registry?
The registry currently lists 9 devices for Gynescope Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gynescope Corp.'s devices?
Among its 9 most recently registered devices, Gynescope Corp. has devices listed in FDA 510(k) (9 devices).
What risk classes do Gynescope Corp.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Gynescope Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gynescope Corp. in the registry?
The most recently registered devices listed for Gynescope Corp. include GYNESCOPE LAPAROSCOPIC TROCARS AND SLEEVES, GYNECOLOGICAL INSTRUMENTATION, GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES and OTT INSUFFLATION FILTER TUBING.