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Pro-Paks MK-7630

by Microspecialities, 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 Number10810003223170 UDI-DI Date2 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  • Withdrawn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

Trade name
Pro-Paks
Generic name
Ophthalmic knife, single-use
Model / Ref / Catalog
MK-7630
Primary DI / UDI-DI
10810003223170
FDA product code
HNN
GMDN term
Ophthalmic knife, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic knife, single-use

Other devices from Microspecialities, Inc.

  • MK8511CB

    Class I

  • MK8510LSK

    Class I

  • 300160

    Class I

  • 300135

    Class I

  • 30020

    Class I

  • MK8507

    Class I

See all devices from Microspecialities, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date

Other properties (9)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No