X-Cel Specialty Contacts
Country not established FDA establishment FEI 3003040707
- Devices
- 19
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 19 devicesCompany details
- FDA FEI number
- 3003040707
- Address
- 2775 Premiere Pkwy Ste 600, DULUTH, GA, 30097
Frequently asked questions
How many devices does X-CEL SPECIALTY CONTACTS have in the registry?
The registry currently lists 19 devices for X-CEL SPECIALTY CONTACTS. Devices recorded under merged duplicate company entries are counted once.
Which registries list X-CEL SPECIALTY CONTACTS's devices?
Among its 19 most recently registered devices, X-CEL SPECIALTY CONTACTS has devices listed in FDA GUDID (19 devices).
What risk classes do X-CEL SPECIALTY CONTACTS's devices fall under?
Among its 19 most recently registered devices, the classes recorded for X-CEL SPECIALTY CONTACTS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from X-CEL SPECIALTY CONTACTS in the registry?
The most recently registered devices listed for X-CEL SPECIALTY CONTACTS include Flexlens Toric, Flexlens Sphere, Flexlens ARC and Flexlens Tricurve Keratoconus.