Cimed Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Cimed Intl., Inc. makes
Cimed International, Inc. manufactures surgical instrumentation and accessories for gynecological procedures, including the Janacek tubo-uterine implantation set for fallopian tube reimplantation, surgical vessel dilators and catheterization tools, and manual surgical instruments for obstetric and gynecological access.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with products listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Janacek Tubo-Uterine Implantation Set Ref K840766
Regimes: 510(k) Registry: 510(k)Surgical Vessel Dilators-Catheriza- Ref K833676
Regimes: 510(k) Registry: 510(k)Certain Manual Surg. Instru. Access Ref K833629
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cimed Intl., Inc. have in the registry?
The registry currently lists 3 devices for Cimed Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cimed Intl., Inc.'s devices?
Among its 3 most recently registered devices, Cimed Intl., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cimed Intl., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cimed Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cimed Intl., Inc. in the registry?
The most recently registered devices listed for Cimed Intl., Inc. include JANACEK TUBO-UTERINE IMPLANTATION SET, SURGICAL VESSEL DILATORS-CATHERIZA- and CERTAIN MANUAL SURG. INSTRU. ACCESS.