← Back to catalogue

Mor-Tight

FDA UDI

Class I (US FDA UDI)

by Tp Orthodontics, Inc.

Identity

Trade Name
Mor-Tight FDA UDI
Generic Name
Orthodontic appliance relief material FDA UDI
Device Name
Store In Cool Dry Place FDA UDI
Model / Reference
100-450 FDA UDI
Description
Store In Cool Dry Place FDA UDI

Identifiers

Primary DI / UDI-DI
00192029049464 FDA UDI
FDA Product Code
EGD FDA UDI
GMDN Term
Orthodontic appliance relief material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6890 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic appliance relief material

Mor-Tight by Tp Orthodontics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic appliance relief material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 98a989a9-af52-4af9-a9df-e6d416b519b6 34 fields · synced May 30, 2026