Surgipro, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Surgipro, Inc. makes
Surgipro, Inc. manufactures sterile single-use trays and kits for surgical and procedural applications, including tracheostomy, dressing changes, laceration/debridement, and central line management. These products are designed to provide organized access to sterile supplies and instruments for wound care, minor surgical procedures, and vascular access.
The company’s products are regulated under the FDA’s Class I and Class II device classifications, with some models requiring 510(k) clearance. These items are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Sterile Tracheostomy Tray Ref K934030
Regimes: 510(k) Registry: 510(k)Sterile Dressing Change Tray Ref K934028
Regimes: 510(k) Registry: 510(k)Sterile Laceration & Debridement Trays Ref K934029
Regimes: 510(k) Registry: 510(k)Sterile Central Line Dressing Tray Ref K934031
Regimes: 510(k) Registry: 510(k)Various Sterile Custom Dressing Trays & Kits Ref K912351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgipro, Inc. have in the registry?
The registry currently lists 5 devices for Surgipro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgipro, Inc.'s devices?
Among its 5 most recently registered devices, Surgipro, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Surgipro, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Surgipro, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgipro, Inc. in the registry?
The most recently registered devices listed for Surgipro, Inc. include STERILE TRACHEOSTOMY TRAY, STERILE DRESSING CHANGE TRAY, STERILE LACERATION & DEBRIDEMENT TRAYS and STERILE CENTRAL LINE DRESSING TRAY.