← Back to catalogue

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
Dental amalgam condenser, reusable FDA UDI
Device Name
HSB - Dycal Instrument/Cavity Liner 4.25'' FDA UDI
Model / Reference
HSB-300114 FDA UDI
Description
HSB - Dycal Instrument/Cavity Liner 4.25'' FDA UDI

Identifiers

Primary DI / UDI-DI
00810132802317 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental amalgam condenser, 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

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: Dental amalgam condenser, reusable

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 Dental amalgam condenser, reusable.

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 3b38af2c-a05c-4b31-ae1c-582ed0f55883 33 fields · synced May 30, 2026