Antalgic Trak AT1000

by Antalgic-Trak

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00860000487504 UDI-DI	Date30 Oct 2018Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Antalgic Trak
Generic Name: Static powered traction system
Model / Reference: AT1000

Primary DI / UDI-DI: 00860000487504
510(k) Number: K042482
FDA Product Code: ITH
GMDN Term: Static powered traction system

Device Class: Class II
Regulation Number: 890.5900
GUDID distribution status: In Commercial Distribution

Other devices from Antalgic-Trak

Antalgic Trak AT-24AF0008B

Class II
Antalgic Trak AT-100

Class II

Properties

Prescription Use
Serial Number
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Expiration Date: No