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Boston Equalens itaflurofocon A

by Bausch & Lomb Incorporated

Boston Equalens itaflurofocon A is a Class III device made by Bausch & Lomb Incorporated, listed in FDA GUDID since 18 Oct 2017 (UDI-DI 00785811435622), 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 Number00785811435622 UDI-DI Date18 Oct 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Boston Equalens
Generic name
Rigid-gas-permeable corrective contact lens, extended-wear
Model / Ref / Catalog
itaflurofocon A, Boston Equalens
Primary DI / UDI-DI
00785811435622
FDA product code
MWL
GMDN term
Rigid-gas-permeable corrective contact lens, extended-wear
Device class
Class III
Regulation number
886.5916
GUDID distribution status
In Commercial Distribution

Related devices

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

Similar devices

Other devices filed under FDA product code MWL (Lens,Contact(Rigid Gas Permeable)-Extended Wear).

Other devices from Bausch & Lomb Incorporated

See all devices from Bausch & Lomb Incorporated →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)