Beta Labs, Inc.
Country not established
- Devices
- 1
What Beta Labs, Inc. makes
Beta Labs, Inc. manufactures the BL1, a hard contact lens designed for vision correction or therapeutic use.
The BL1 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
BL1 (Hard Contact Lens) Ref K864343
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beta Labs, Inc. have in the registry?
The registry currently lists 1 device for Beta Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beta Labs, Inc.'s devices?
Among its 1 most recently registered device, Beta Labs, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Beta Labs, Inc. in the registry?
The most recently registered devices listed for Beta Labs, Inc. include BL1 (HARD CONTACT LENS).