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Mk-700700-20

by Microspecialities, Inc.

Mk-700700-20 is a Class I device made by Microspecialities, Inc., listed in FDA GUDID since 3 Jan 2019 (UDI-DI 10810003222357), 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 Number10810003222357 UDI-DI Date3 Jan 2019ListedStatusListed 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  • Withdrawn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

Generic name
Keratome blade, single-use
Model / Ref / Catalog
MK-700700-20
Description
MicroKeratome Blades, MORIA M2 minus 20. Have the ultimate control of corneal flap thickness while using a single head. Range from -40 to +20 microns. 10/bx
Primary DI / UDI-DI
10810003222357
FDA product code
HNO
GMDN term
Keratome blade, single-use
Device class
Class I
Regulation number
886.4370
GUDID distribution status
In Commercial Distribution
Size
Angle — -20 degree

Related devices

Category: Keratome blade, single-use

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
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)