Tanaka Dental AT3

by Nordent Manufacturing Inc

Tanaka Dental AT3 is a Class I device made by Nordent Manufacturing Inc, listed in FDA GUDID since 20 Jul 2020 (UDI-DI 00840018648739), registry data as of 23 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00840018648739 UDI-DI	Date20 Jul 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00840018648739

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Tanaka Dental
Generic name: Dental restoration carver, amalgam, reusable
Model / reference: AT3

Primary DI / UDI-DI: 00840018648739
FDA product code: EKH
GMDN term: Dental restoration carver, amalgam, reusable

Device class: Class I
Regulation number: 872.4565
GUDID distribution status: In Commercial Distribution

Similar devices

Other devices filed under FDA product code EKH (Carver, Dental Amalgam, Operative).

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Properties

Sterilise before use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (11, all answered No)