Vitalitec Int'l., Inc.
Country not established FDA establishment FEI 3002539629
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Vitalitec Int'l., Inc. makes
Vitalitec Int'l., Inc. manufactures titanium hemostatic clips.
The company's devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Titanium Hemostatic Clip Ref K981645
510(k) 510(k)
Company details
- FDA FEI number
- 3002539629
- Address
- 10 Cordage Park Cir Suite 100, Plymouth, MA, 02360
Frequently asked questions
How many devices does VITALITEC INT'L., INC. have in the registry?
The registry currently lists 1 device for VITALITEC INT'L., INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VITALITEC INT'L., INC.'s devices?
Among its 1 most recently registered device, VITALITEC INT'L., INC. has devices listed in FDA 510(k) (1 device).
What risk classes do VITALITEC INT'L., INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for VITALITEC INT'L., INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VITALITEC INT'L., INC. in the registry?
The most recently registered devices listed for VITALITEC INT'L., INC. include TITANIUM HEMOSTATIC CLIP.