Airperm, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Airperm, Inc. makes
Airperm, Inc. manufactures rigid gas permeable contact lenses designed for daily wear, including multifocal and orthokeratology (ortho-k) variants. Their products are formulated with siflufocon A, a material intended for extended comfort and vision correction.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device authorisation requirements.
Catalogue
Contact Lens Ref K941883
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Airperm (Siflufocon A) Rigid Gas Permeable Ok Contact Lenses For Daily Wear Orthokeratology Ref K973697
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Airperm, Inc. have in the registry?
The registry currently lists 3 devices for Airperm, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airperm, Inc.'s devices?
Among its 3 most recently registered devices, Airperm, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Airperm, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Airperm, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Airperm, Inc. in the registry?
The most recently registered devices listed for Airperm, Inc. include CONTACT LENS, AIRPERM(SIFLUFOCON A) RIGID GAS PERMEABLE MULTIFOCAL CONTACT LENSES FOR DAILY WEAR and AIRPERM (SIFLUFOCON A) RIGID GAS PERMEABLE OK CONTACT LENSES FOR DAILY WEAR ORTHOKERATOLOGY.