← Back to catalogue

HuFriedyGroup

FDA UDI

Class II (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
HuFriedyGroup FDA UDI
Generic Name
Dental abrasive air jet system handpiece FDA UDI
Device Name
DEMO- PWR Air Perio Handpiece FDA UDI
Model / Reference
D-APHPPERIO FDA UDI
Description
DEMO- PWR Air Perio Handpiece FDA UDI

Identifiers

Primary DI / UDI-DI
10889950143893 FDA UDI
510(k) Number
K231391 FDA UDI
FDA Product Code
KOJ FDA UDI
GMDN Term
Dental abrasive air jet system handpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6080 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental abrasive air jet system handpiece

HuFriedyGroup by Hu-Friedy Mfg Co., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive air jet system handpiece.

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 f253c3b4-fdfd-45da-880c-b59cbd037dbf 35 fields · synced May 30, 2026