Skip to content

Pro-Paks®️ Mk-301

by Microspecialities, Inc.

Pro-Paks®️ Mk-301 is a Class II device made by Microspecialities, Inc., listed in FDA GUDID since 30 Oct 2018 (UDI-DI 10810003220070), 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 Number10810003220070 UDI-DI Date30 Oct 2018ListedStatusListed 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  • Withdrawn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
Pro-Paks®️
Generic name
Ophthalmic sponge
Model / Ref / Catalog
MK-301
Primary DI / UDI-DI
10810003220070
FDA product code
HOZ
GMDN term
Ophthalmic sponge
Device class
Class II
Regulation number
886.4790
GUDID distribution status
In Commercial Distribution
Size
Lumen/Inner Diameter — 11.5 Millimeter

Related devices

Category: Ophthalmic sponge

Similar devices in this category

Other devices filed under Ophthalmic sponge.

Other devices from Microspecialities, Inc.

  • MK8511CB

    Class I

  • MK8510LSK

    Class I

  • 300160

    Class I

  • 300135

    Class I

See all devices from Microspecialities, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)