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House Brand Dentistry

FDA UDI

Class I (US FDA UDI)

by Frontier Dental Supply Inc

Identity

Trade Name
House Brand Dentistry FDA UDI
Generic Name
Cast/plaster knife FDA UDI
Device Name
HSB - Plaster Knife #12 2'' FDA UDI
Model / Reference
HSB-300158 FDA UDI
Description
HSB - Plaster Knife #12 2'' FDA UDI

Identifiers

Primary DI / UDI-DI
00810132802737 FDA UDI
FDA Product Code
EMF FDA UDI
GMDN Term
Cast/plaster knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Cast/plaster knife

House Brand Dentistry by Frontier Dental Supply Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cast/plaster knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7a28376b-68c2-4f43-a08c-b5f141d4d354 33 fields · synced May 31, 2026