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Flexible Partial Resin

FDA UDI

Class II (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name
Flexible Partial Resin FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Flexible Partial Resin Shade G3 FDA UDI
Model / Reference
70-1164-RSN0009 FDA UDI
Description
Flexible Partial Resin Shade G3 FDA UDI

Identifiers

Catalog Number
70-1164-RSN0009 FDA UDI
Primary DI / UDI-DI
D745701164RSN00090 FDA UDI
510(k) Number
K250302 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

No

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

Flexible Partial Resin by Prismatik Dentalcraft, Inc. — 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

Sources (1)

  • FDA UDI da405aaa-f570-4f7d-954b-aa843063a739 35 fields · synced May 30, 2026