← Back to catalogue

Enamelast

FDA UDI

Class II (US FDA UDI)

by Ultradent Products, Inc.

Identity

Trade Name
Enamelast FDA UDI
Generic Name
Dental coating, tooth-desensitizing, professional FDA UDI
Device Name
Enamelast Syringe 2pk - Walterberry FDA UDI
Model / Reference
4521 FDA UDI
Description
Enamelast Syringe 2pk - Walterberry FDA UDI

Identifiers

Catalog Number
4521 FDA UDI
Primary DI / UDI-DI
00883205103185 FDA UDI
FDA Product Code
LBH FDA UDI
GMDN Term
Dental coating, tooth-desensitizing, professional 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

No

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: Dental coating, tooth-desensitizing, professional

Enamelast by Ultradent Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental coating, tooth-desensitizing, professional.

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 2b7ddcbd-6c1e-48ab-99eb-53e74b13720f 36 fields · synced May 31, 2026