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Rocoto

by Rocoto Inc. 2 variants

Rocoto is a Class I device made by Rocoto Inc., listed in FDA GUDID since 26 Feb 2026 (UDI-DI 00860015454744), 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 Number00860015454744 UDI-DI Date26 Feb 2026ListedStatusListed 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  • Withdrawn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

Generic name
Surgical video camera
Model / reference
SL11 device - Wireless Camera - MDMP1_SL11_1STE12
Primary DI / UDI-DI
00860015454744
FDA product code
KQM
GMDN term
Surgical video camera
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KQM (Camera, Surgical And Accessories).

Other devices from Rocoto Inc.

See all devices from Rocoto Inc. →

Properties

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