Accu-Lens, Inc.
Country not established FDA establishment FEI 1720959
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Company details
- FDA FEI number
- 1720959
- Address
- 13301 W 43rd Dr Unit 4, Golden, CO, 80403
Frequently asked questions
How many devices does ACCU-LENS, INC. have in the registry?
The registry currently lists 1 device for ACCU-LENS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ACCU-LENS, INC.'s devices?
Among its 1 most recently registered device, ACCU-LENS, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do ACCU-LENS, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for ACCU-LENS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ACCU-LENS, INC. in the registry?
The most recently registered devices listed for ACCU-LENS, INC. include NewVision SC (tisilfocon A) Scleral Lens; NewVision SC Daily Wear Ortho-K (tisilfocon A) Corneo-Scleral Lens.