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SciPharm Dental Etching Agent Bottle, Non-Boxed

FDA UDI

Class II (US FDA UDI)

by Scientific Pharmaceuticals, Inc.

Identity

Trade Name
SciPharm Dental Etching Agent Bottle, Non-Boxed FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Enamel Conditioner FDA UDI
Model / Reference
SP 50-013 N FDA UDI
Description
Enamel Conditioner FDA UDI

Identifiers

Catalog Number
50-013 FDA UDI
Primary DI / UDI-DI
D801SP50013N1 FDA UDI
510(k) Number
K872569 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

Yes

FDA UDI

Category: Dental etching solution

SciPharm Dental Etching Agent Bottle, Non-Boxed by Scientific Pharmaceuticals, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f631fb5-de4c-4dda-9e95-01b8eb1adfd1 37 fields · synced Jun 1, 2026