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MSI Precision Specialty Instruments 19-173

by Med Saver, Inc.

MSI Precision Specialty Instruments 19-173 is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 1 Aug 2025 (UDI-DI 00194613026189), 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 Number00194613026189 UDI-DI Date1 Aug 2025ListedStatusListed 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  • Withdrawn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
MSI Precision Specialty Instruments
Generic name
Ophthalmic conformer
Model / reference
19-173
Primary DI / UDI-DI
00194613026189
FDA product code
HOY
GMDN term
Ophthalmic conformer
Device class
Class I
Regulation number
886.4750
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic conformer

Similar devices

Other devices filed under FDA product code HOY (Shield, eye, ophthalmic (including sunlamp protective eyewear and post-mydriatic eyewear)).

Other devices from Med Saver, Inc.

See all devices from Med Saver, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)