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AccuPlan System

FDA UDI

Class II (US FDA UDI)

by Medcad

Identity

Trade Name
AccuPlan System FDA UDI
Generic Name
Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI
Device Name
MANDIBLE RECONSTRUCTION, SURGICAL PLANNING KIT W/ ACCUPLATE 3DTI AND TITANIUM GUIDES BUNDLE FDA UDI
Model / Reference
ZB-KTP130 FDA UDI
Description
MANDIBLE RECONSTRUCTION, SURGICAL PLANNING KIT W/ ACCUPLATE 3DTI AND TITANIUM GUIDES BUNDLE FDA UDI

Identifiers

Primary DI / UDI-DI
00810007633183 FDA UDI
FDA Product Code
JEY FDA UDI
LLZ FDA UDI
DZJ FDA UDI
GMDN Term
Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 FDA UDI
892.2050 FDA UDI
872.4120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial fixation plate, non-bioabsorbable, non-customizedDental milling system, CAD/CAM, laboratoryCustom-made organ/bone anatomy model/surgical guide kit

AccuPlan System by Medcad — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made organ/bone anatomy model/surgical guide kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medcad

Sources (1)

  • FDA UDI 49ed41ec-839e-4835-b851-28e90c01f7fc 34 fields · synced May 30, 2026