Autolign 1.0

by Diorco Co., Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08800099800008 UDI-DI	Date25 Aug 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name: Autolign
Generic Name: Dental milling system, CAD/CAM, laboratory
Model / Reference: 1.0

Primary DI / UDI-DI: 08800099800008
GMDN Term: Dental milling system, CAD/CAM, laboratory

GUDID distribution status: In Commercial Distribution

Other devices from Diorco Co., Ltd.

Dicaon 4D 1.0

Not classified
Autolign

Class II

Properties

Convenience Kit
Serial Number
Manufacturing Date

Other properties (11)

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