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Naturally White

FDA UDI

Class II (US FDA UDI)

by Park Dental Research Corp

Identity

Trade Name
Naturally White FDA UDI
Generic Name
Orthodontic progressive aligner FDA UDI
Device Name
Naturally White Retainer FDA UDI
Model / Reference
NW-RET FDA UDI
Description
Naturally White Retainer FDA UDI

Identifiers

Primary DI / UDI-DI
D769NWRET0 FDA UDI
FDA Product Code
NXC FDA UDI
GMDN Term
Orthodontic progressive aligner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic progressive aligner

Naturally White by Park Dental Research Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic progressive aligner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bfe6ab0b-074e-489b-b354-9c664fc4276e 34 fields · synced May 31, 2026