Surgipro Central, Inc.
Country not established
- Devices
- 1
What Surgipro Central, Inc. makes
Surgipro Central, Inc. manufactures non-sterile custom surgical trays and kits designed for procedural use in operating rooms and clinical settings.
These products are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Various Non-Sterile Custom Trays/Kits Ref K924690
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgipro Central, Inc. have in the registry?
The registry currently lists 1 device for Surgipro Central, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgipro Central, Inc.'s devices?
Among its 1 most recently registered device, Surgipro Central, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Surgipro Central, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgipro Central, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgipro Central, Inc. in the registry?
The most recently registered devices listed for Surgipro Central, Inc. include VARIOUS NON-STERILE CUSTOM TRAYS/KITS.