Spinamic 25-4600-2

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08809766910316 UDI-DI	Date18 Mar 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Spinamic
Generic Name: Multiple spinal region orthosis
Model / Ref / Catalog: 25-4600-2, VNTC Spinamic Replacement Pads #2

Primary DI / UDI-DI: 08809766910316
FDA Product Code: KTD
GMDN Term: Multiple spinal region orthosis

Device Class: Class I
Regulation Number: 890.3490
GUDID distribution status: In Commercial Distribution

Other devices from Value&Trust

Spinamic 25-4600-1

Class I
Spinamic 25-4600-3

Class I

Properties

Prescription Use
Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (10)

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