D.D. Surgical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What D.D. Surgical, Inc. makes
D.D. Surgical, Inc. manufactures the LASEVAC, a device designed for surgical smoke evacuation and laser plume containment during procedures involving lasers or electrosurgery.
The LASEVAC is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
IOL Implantation Forceps Ref K883197
510(k) 510(k)Lasevac Ref K951490
510(k) 510(k)
Frequently asked questions
How many devices does D.D. Surgical, Inc. have in the registry?
The registry currently lists 2 devices for D.D. Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D.D. Surgical, Inc.'s devices?
Among its 2 most recently registered devices, D.D. Surgical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do D.D. Surgical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for D.D. Surgical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from D.D. Surgical, Inc. in the registry?
The most recently registered devices listed for D.D. Surgical, Inc. include IOL IMPLANTATION FORCEPS and LASEVAC.