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Oxfore100

by Paragon Vision Sciences

Oxfore100 is a Class II device made by Paragon Vision Sciences, listed in FDA GUDID since 18 Sep 2023 (UDI-DI B22225), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB22225 UDI-DI Date18 Sep 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Rigid-gas-permeable corrective contact lens, daily-wear, non-customized
Model / reference
Oxfore100
Primary DI / UDI-DI
B22225
FDA product code
HQD
GMDN term
Rigid-gas-permeable corrective contact lens, daily-wear, non-customized
Device class
Class II
Regulation number
886.5916
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid-gas-permeable corrective contact lens, daily-wear

Similar devices

Other devices filed under FDA product code HQD (Lens, Contact (Other Material) - Daily).

Other devices from Paragon Vision Sciences

See all devices from Paragon Vision Sciences →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)