Femspec LLC
United StatesFDA applicant, unverified
- Devices
- 4
What Femspec LLC makes
Femspec LLC manufactures single-use and reusable instruments for gynecological procedures, including endometrial suction curettes, disposable sterile vaginal specula, and endocervical curettes. These devices are designed for diagnostic and procedural applications in clinical settings, such as endometrial sampling and cervical examinations.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) clearance registry. The products are intended for use in the United States.
Catalogue
Femtest Endometrial Suction Curette, Model Ft-1 Ref K051294
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Femspec Disposable Vaginal Speculum Ref K041757
Regimes: 510(k) Registry: 510(k)Femecc Endocervical Curette Ref K060320
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Femspec LLC have in the registry?
The registry currently lists 4 devices for Femspec LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Femspec LLC's devices?
Among its 4 most recently registered devices, Femspec LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do Femspec LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Femspec LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Femspec LLC in the registry?
The most recently registered devices listed for Femspec LLC include FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1, FEMSPCE-S DISPOSABLE STERILE VAGINAL SPECULUM, MODEL ST-I, FEMSPEC DISPOSABLE VAGINAL SPECULUM and FEMECC ENDOCERVICAL CURETTE.