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Goldman-Fox Anterior Scaler

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
GOLDMAN-FOX ANTERIOR SCALER FDA UDI
Generic Name
Manual dental scaler, reusable FDA UDI
Device Name
GOLDMAN-FOX SCALER #21/JACQUETTE CURETTE SMALL BLADE/TAPERED POINT BLADE FDA UDI
Model / Reference
1102-SCGF21 FDA UDI
Description
GOLDMAN-FOX SCALER #21/JACQUETTE CURETTE SMALL BLADE/TAPERED POINT BLADE FDA UDI

Identifiers

Catalog Number
1102-SCGF21 FDA UDI
Primary DI / UDI-DI
00192896050525 FDA UDI
FDA Product Code
EMK FDA UDI
GMDN Term
Manual dental scaler, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual dental scaler, reusable

Goldman-Fox Anterior Scaler by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual dental scaler, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 306d55c7-7d69-4ace-a9c5-e79f75552db3 36 fields · synced Jun 1, 2026