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ClearCut® - Intrepid 8065982265

by Alcon Laboratories, Inc.

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

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 Number00380659822650 UDI-DI Date18 Aug 2020ListedStatusListed GUDID: 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  • Withdrawn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
ClearCut®; Intrepid
Generic Name
Ophthalmic knife, single-use
Model / Reference
8065982265
Primary DI / UDI-DI
00380659822650
FDA Product Code
HNN
GMDN Term
Ophthalmic knife, single-use
Models / Variants
Intrepid 8065982265
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic knife, single-use

Other devices from Alcon Laboratories, Inc.

See all devices from Alcon Laboratories, Inc. →

Properties

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

Other properties (7)

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