Skip to content

Humero Tech C1 HD

by Titin Km Biomedical Corp.

Humero Tech C1 HD (A2-0000) is a virtual-display rehabilitation system (FDA Class I; FDA product code ION, Exerciser, Non-Measuring) made by Titin Km Biomedical Corp., listed in FDA GUDID since 11 Dec 2024 (UDI-DI 00860010519912), 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 Number00860010519912 UDI-DI Date11 Dec 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  • Withdrawn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
Humero Tech
Generic name
Virtual-display rehabilitation system, passive-support, upper-limb
Model / Ref / Catalog
C1 HD, A2-0000
Primary DI / UDI-DI
00860010519912
FDA product code
ION
GMDN term
Virtual-display rehabilitation system, passive-support, upper-limb
Device class
Class I
Regulation number
890.5370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Virtual-display rehabilitation system, passive-support, upper-limb

Similar devices

Other devices filed under FDA product code ION (Exerciser, Non-Measuring).

Other devices from Titin Km Biomedical Corp.

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)