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Sunoptic Technologies Camera System

by Sunoptic Technologies

Sunoptic Technologies Camera System is a Class I device made by Sunoptic Technologies, listed in FDA GUDID since 9 May 2017 (UDI-DI M678CS0), 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 NumberM678CS0 UDI-DI Date9 May 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sunoptic Technologies
Generic name
Surgical video camera
Model / reference
Camera System
Primary DI / UDI-DI
M678CS0
FDA product code
FWF, KQM
GMDN term
Surgical video camera
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical video camera

Similar devices in this category

Other devices filed under Surgical video camera.

Other devices from Sunoptic Technologies

See all devices from Sunoptic Technologies →

Properties

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