AccuPlan® System ZB-K000-R

AccuPlan® System ZB-K000-R is a Class II device made by Medcad, listed in FDA GUDID since 5 May 2022 (UDI-DI 00810007630656), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00810007630656 UDI-DI	Date5 May 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00810007630656

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: AccuPlan® System
Generic name: Dental milling system, CAD/CAM, laboratory
Model / Ref / Catalog: ZB-K000-R

Primary DI / UDI-DI: 00810007630656
FDA product code: DZJ, LLZ
GMDN term: Dental milling system, CAD/CAM, laboratory

Device class: Class II
Regulation number: 872.4120, 892.2050
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from Medcad

See all devices from Medcad →

Properties

Sterilise before use
Single use
Prescription use
Lot / batch number
Serial number

Other properties (10, all answered No)