Surgemed Marketing, Inc.
Country not established
- Devices
- 1
What Surgemed Marketing, Inc. makes
Surgemed Marketing, Inc. manufactures the Forder Retractor, a surgical instrument designed to provide exposure and retraction during procedures.
The Forder Retractor is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Forder Retractor Ref K811973
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgemed Marketing, Inc. have in the registry?
The registry currently lists 1 device for Surgemed Marketing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgemed Marketing, Inc.'s devices?
Among its 1 most recently registered device, Surgemed Marketing, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Surgemed Marketing, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgemed Marketing, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Surgemed Marketing, Inc. in the registry?
The most recently registered devices listed for Surgemed Marketing, Inc. include FORDER RETRACTOR.