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Ortho-Tain, Inc

FDA UDI

Class II (US FDA UDI)

by Ortho-Tain, Inc

Identity

Trade Name
Ortho-Tain, Inc FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Device Name
SNORE CURE FDA UDI
Model / Reference
SNORE CURE FDA UDI
Description
SNORE CURE FDA UDI

Identifiers

Catalog Number
00S FDA UDI
Primary DI / UDI-DI
D866SC0 FDA UDI
FDA Product Code
LRK FDA UDI
GMDN Term
Orthodontic retainer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5570 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

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

Category: Orthodontic retainer

Ortho-Tain, Inc by Ortho-Tain, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortho-Tain, Inc

Sources (1)

  • FDA UDI 7d0e9bdc-711e-434c-bed8-27b41e2121ac 34 fields · synced May 30, 2026