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Vitreon Perfluorophenanthrene Intraocular Fluid

by Air Products & Chemicals, Inc.

PMA P910068

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 30 Sep 1997

PMA

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP910068 Date30 Sep 1997Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA PMA Withdrawn

Specification

PMA

Full name
Vitreon(R)
Generic Name
Fluid, intraocular
PMA Number
FDA Product Code
LWL
Device Class
Class III
Regulation
21 CFR Part 886.4275
Advisory Committee
Ophthalmic
FDA Decision
APWD Approval withdrawn

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