Taglus Tuff VS1083

by Laxmi Dental Limited

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	Number08906139322414 UDI-DI	Date9 Jan 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Taglus Tuff
Generic Name: Dental appliance fabrication material, thermoplastic
Model / Reference: VS1083

Primary DI / UDI-DI: 08906139322414
FDA Product Code: KMY
GMDN Term: Dental appliance fabrication material, thermoplastic

Device Class: Class I
Regulation Number: 872.5525
GUDID distribution status: In Commercial Distribution

Other devices from Laxmi Dental Limited

Taglus Aligner Removal Tool VS540

Class I
Taglus Ortho Chewies VS539

Class I
Taglus Tuff VS304

Class I
Taglus Model Resin Odourless VS706

Class I

Properties

Single Use
Premarket Exempt
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (9)

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