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Alcon GRIESHABER REVOLUTION 708.12

by Alcon Laboratories, Inc.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07612717059047 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Alcon GRIESHABER REVOLUTION
Generic Name
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
Model / Reference
708.12
Primary DI / UDI-DI
07612717059047
FDA Product Code
HQC, HNR
GMDN Term
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
Device Class
Class II
Regulation Number
886.4670, 886.4350
GUDID distribution status
Not in Commercial Distribution
Size
Needle Gauge — 20 Gauge

Other devices from Alcon Laboratories, Inc.

See all devices from Alcon Laboratories, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No