Synovis Life Technologies, Inc. (Baxter International Inc.)
Country not established
- Devices
- 1
What Synovis Life Technologies, Inc. (Baxter International Inc.) makes
Synovis Life Technologies manufactures Peri-Strips Dry, a collagen-based matrix with Secure Grip Technology designed for soft tissue reinforcement and wound coverage in surgical applications.
The company’s portfolio is regulated under FDA Class II devices, with Peri-Strips Dry authorised via the 510(k) pathway. The product is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Synovis Life Technologies, Inc. (Baxter International Inc.) have in the registry?
The registry currently lists 1 device for Synovis Life Technologies, Inc. (Baxter International Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Synovis Life Technologies, Inc. (Baxter International Inc.)'s devices?
Among its 1 most recently registered device, Synovis Life Technologies, Inc. (Baxter International Inc.) has devices listed in FDA 510(k) (1 device).
What risk classes do Synovis Life Technologies, Inc. (Baxter International Inc.)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Synovis Life Technologies, Inc. (Baxter International Inc.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Synovis Life Technologies, Inc. (Baxter International Inc.) in the registry?
The most recently registered devices listed for Synovis Life Technologies, Inc. (Baxter International Inc.) include Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG).