Vlm Surgical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Vlm Surgical, Inc. makes
Vlm Surgical, Inc. manufactures THE SUTURER, a device designed for automated tissue suturing, and Kilejian Circumcision Template [THE DOME], a precision guide for circumcision procedures.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
The Suturer Ref K842912
510(k) 510(k)Kilejian Circumcision Template [The Dome] Ref K945949
510(k) 510(k)
Frequently asked questions
How many devices does Vlm Surgical, Inc. have in the registry?
The registry currently lists 2 devices for Vlm Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vlm Surgical, Inc.'s devices?
Among its 2 most recently registered devices, Vlm Surgical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vlm Surgical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vlm Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vlm Surgical, Inc. in the registry?
The most recently registered devices listed for Vlm Surgical, Inc. include THE SUTURER and KILEJIAN CIRCUMCISION TEMPLATE [THE DOME].