Biotime, Inc.
Country not established
- Devices
- 1
What Biotime, Inc. makes
Biotime, Inc. manufactures PREMVIA, a Class II medical device designed for obstetric use, specifically intended for the prevention of preterm birth in high-risk pregnancies.
PREMVIA is regulated under the U.S. Food and Drug Administration’s 510(k) pathway and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Premvia Ref K134037
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biotime, Inc. have in the registry?
The registry currently lists 1 device for Biotime, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biotime, Inc.'s devices?
Among its 1 most recently registered device, Biotime, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Biotime, Inc. in the registry?
The most recently registered devices listed for Biotime, Inc. include PREMVIA.