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PRO3DURE GR-14.2 denture HI

FDA UDI

Class II (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
PRO3DURE GR-14.2 denture HI FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Printodent GR-14.2 denture HI FDA UDI
Model / Reference
1kg - Deep-Pink FDA UDI
Description
Printodent GR-14.2 denture HI FDA UDI

Identifiers

Primary DI / UDI-DI
EPRCD1001313 FDA UDI
510(k) Number
K210298 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, resin

PRO3DURE GR-14.2 denture HI by Pro3Dure Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pro3Dure Medical

Sources (1)

  • FDA UDI 832a2473-428a-4d68-a7ed-0abf752ae15e 36 fields · synced Jun 1, 2026