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MediVision MVA445

by Medivision, Inc.

MediVision MVA445 is a Class II device made by Medivision, Inc., listed in FDA GUDID since 14 Dec 2016 (UDI-DI 00851328007093), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851328007093 UDI-DI Date14 Dec 2016ListedStatusListed 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  • Withdrawn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
MediVision
Generic name
Rigid optical sinoscope
Model / Ref / Catalog
MVA445
Primary DI / UDI-DI
00851328007093
FDA product code
HRX, EOB
GMDN term
Rigid optical sinoscope
Device class
Class II
Regulation number
888.1100, 874.4760
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid optical arthroscope, reusableRigid optical sinoscope

Similar devices

Other devices filed under FDA product code HRX (Arthroscope).

Other devices from Medivision, Inc.

See all devices from Medivision, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)