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Prosidio L.E. All-in-one endoscopy system V1.0

by Prosidio LLC

Prosidio L.E. All-in-one endoscopy system V1.0 (LE001) is a Class I device made by Prosidio LLC, listed in FDA GUDID since 6 Jun 2021 (UDI-DI 00860006918705), 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 Number00860006918705 UDI-DI Date6 Jun 2021ListedStatusListed 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  • Withdrawn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
Prosidio
Generic name
Endoscopic video image processing/light source system
Model / Ref / Catalog
L.E. All-in-one endoscopy system V1.0, LE001
Primary DI / UDI-DI
00860006918705
FDA product code
FWL
GMDN term
Endoscopic video image processing/light source system
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscope video cameraEndoscopic video image processing/light source system

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)