← Back to catalogue

House Brand Dentistry

FDA UDI

Class II (US FDA UDI)

by Frontier Dental Supply Inc

Identity

Trade Name
House Brand Dentistry FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
2.75" x 10" - Paper/Blue Film Self-Sealing Sterilization Pouch 200/Bx FDA UDI
Model / Reference
HSB-100521 FDA UDI
Description
2.75" x 10" - Paper/Blue Film Self-Sealing Sterilization Pouch 200/Bx FDA UDI

Identifiers

Primary DI / UDI-DI
00810132800269 FDA UDI
510(k) Number
K071886 FDA UDI
K143637 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

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

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: Sterilization packaging, single-use

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

Similar devices

Also classified as Sterilization packaging, single-use.

Cleared under the same submission

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 35019e84-0bcc-48e9-8665-53d7299b449b 34 fields · synced May 29, 2026