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Amimon HM11 Device - MDWL1_HM11

by Rocoto Inc.

Amimon HM11 Device - MDWL1_HM11 is a Class I device made by Rocoto Inc., listed in FDA GUDID since 24 Jun 2025 (UDI-DI 00860014100680), 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 Number00860014100680 UDI-DI Date24 Jun 2025ListedStatusListed 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  • Withdrawn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
Amimon
Generic name
Head-worn lamp
Model / Ref / Catalog
HM11 Device - MDWL1_HM11, MDWL1_HM11
Primary DI / UDI-DI
00860014100680
FDA product code
HPP
GMDN term
Head-worn lamp
Device class
Class I
Regulation number
886.4335
GUDID distribution status
In Commercial Distribution

Related devices

Category: Head-worn lamp

Similar devices

Other devices filed under FDA product code HPP (Headlamp, Operating, Battery-Operated).

Other devices from Rocoto Inc.

See all devices from Rocoto Inc. →

Properties

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