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multiSTATION™ 080780

by LSI Solutions, Inc.

multiSTATION™ 080780 is a Class I device made by LSI Solutions, Inc., listed in FDA GUDID since 27 Sep 2024 (UDI-DI 00850012846369), 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 Number00850012846369 UDI-DI Date27 Sep 2024ListedStatusListed 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  • Withdrawn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
multiSTATION™
Generic name
Surgical instrument assist arm system structural component
Model / Ref / Catalog
080780
Primary DI / UDI-DI
00850012846369
FDA product code
MDM
GMDN term
Surgical instrument assist arm system structural component
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical instrument assist arm system structural component

Similar devices

Other devices filed under FDA product code MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE).

Other devices from LSI Solutions, Inc.

See all devices from LSI Solutions, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)