Suture Ease, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3009956343
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009956343
- Address
- 908 C Street, Galt, CA, 95632
Frequently asked questions
How many devices does SUTURE EASE, INC. have in the registry?
The registry currently lists 1 device for SUTURE EASE, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SUTURE EASE, INC.'s devices?
Among its 1 most recently registered device, SUTURE EASE, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do SUTURE EASE, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for SUTURE EASE, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SUTURE EASE, INC. in the registry?
The most recently registered devices listed for SUTURE EASE, INC. include CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor.