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Ortho Resin

FDA UDI

Class II (US FDA UDI)

by American Tooth Industries

Identity

Trade Name
ORTHO RESIN FDA UDI
Generic Name
Dental acrylic resin FDA UDI
Device Name
ORTHO RESIN KIT/W PINK LIQUID FDA UDI
Model / Reference
072-05-0001 FDA UDI
Description
ORTHO RESIN KIT/W PINK LIQUID FDA UDI

Identifiers

Primary DI / UDI-DI
D772ATI0500010 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental acrylic resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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 acrylic resin

Ortho Resin by American Tooth Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental acrylic resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 856465fb-290a-423f-9efc-146ddc8b588f 33 fields · synced Jun 8, 2026