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Proflex

FDA UDI

Class II (US FDA UDI)

by Keystone Industries

Identity

Trade Name
Proflex FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
NFC Clear Resin FDA UDI
Model / Reference
9146200 FDA UDI
Description
NFC Clear Resin FDA UDI

Identifiers

Catalog Number
9146200 FDA UDI
Primary DI / UDI-DI
H66891462001 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 960 Gram FDA UDI

Category: Dental appliance fabrication material, resin

Proflex by Keystone Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keystone Industries

Sources (1)

  • FDA UDI 05d1ecba-b068-4e04-9bc8-1c8c8cd9a9f6 36 fields · synced Jun 9, 2026