Bio-Lipid, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Bio-Lipid, Inc. makes
Bio-Lipid, Inc. manufactures ophthalmic warming devices, specifically the EYEFEEL OPHTHALMIC WARMER, designed for pre-procedural eye temperature regulation.
The company’s portfolio is regulated under FDA’s Class I device classification, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Eyefeel Ophthalmic Warmer Ref K021843
Regimes: 510(k) Registry: 510(k)Eyefeel Ophthalmic Warmer Ref K082087
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bio-Lipid, Inc. have in the registry?
The registry currently lists 2 devices for Bio-Lipid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bio-Lipid, Inc.'s devices?
Among its 2 most recently registered devices, Bio-Lipid, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bio-Lipid, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bio-Lipid, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bio-Lipid, Inc. in the registry?
The most recently registered devices listed for Bio-Lipid, Inc. include EYEFEEL OPHTHALMIC WARMER.