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NovaBright

FDA UDI

Class II (US FDA UDI)

by Nanova Biomaterials Inc

Identity

Trade Name
NovaBright FDA UDI
Generic Name
Fluoride gel FDA UDI
Device Name
0.25 mL 5% Sodium Fluoride Varnish (Cherry) FDA UDI
Model / Reference
14238-252 FDA UDI
Description
0.25 mL 5% Sodium Fluoride Varnish (Cherry) FDA UDI

Identifiers

Primary DI / UDI-DI
00816537021391 FDA UDI
FDA Product Code
LBH FDA UDI
GMDN Term
Fluoride gel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3260 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluoride gel

NovaBright by Nanova Biomaterials Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluoride gel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9eff87d0-be60-4ff8-9d9c-8d81a261e7f7 34 fields · synced Jun 1, 2026