W.O.M. GmbH
GermanyFDA 510(k) applicant, unverified
- Devices
- 3
What W.O.M. GmbH makes
W.O.M. GmbH manufactures electronic and pneumatic surgical devices for laparoscopic and gynecological procedures, including the WOM Laparoflator Electronic for insufflation, the Surgiflator 20 for gas insufflation control, and the WOM Hysteroflator OP for hysteroscopic fluid management.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance in the United States. The company is based in the US.
Catalogue
Wom Laparoflator Electronic Ref K921086
510(k) 510(k)Surgiflator 20 Ref K950035
510(k) 510(k)Wom Hysteroflator Op Ref K922632
510(k) 510(k)
Frequently asked questions
How many devices does W.O.M. GmbH have in the registry?
The registry currently lists 3 devices for W.O.M. GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list W.O.M. GmbH's devices?
Among its 3 most recently registered devices, W.O.M. GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do W.O.M. GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for W.O.M. GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from W.O.M. GmbH in the registry?
The most recently registered devices listed for W.O.M. GmbH include WOM LAPAROFLATOR ELECTRONIC, SURGIFLATOR 20 and WOM HYSTEROFLATOR OP.