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Hu-Friedy MFG Co., LLC.

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
Hu-Friedy MFG Co., LLC. FDA UDI
Generic Name
Periodontal knife FDA UDI
Device Name
1/2 Orban DE Knife, Long Satin Steel Hdl FDA UDI
Model / Reference
KO1/2IU6 FDA UDI
Description
1/2 Orban DE Knife, Long Satin Steel Hdl FDA UDI

Identifiers

Primary DI / UDI-DI
10889950014520 FDA UDI
FDA Product Code
EMO FDA UDI
GMDN Term
Periodontal knife 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

No

FDA UDI

Category: Periodontal knife

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

Similar devices

Also classified as Periodontal knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 501eef84-dcd6-4c21-885c-9b17b3602fd3 34 fields · synced May 30, 2026