Z21

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name: Z21 FDA UDI
Generic Name: Periosteal elevator, reusable FDA UDI
Device Name: P9X Periosteal with #6 short handle FDA UDI
Model / Reference: SPECIAL7 FDA UDI
Description: P9X Periosteal with #6 short handle FDA UDI

Identifiers

Primary DI / UDI-DI: 10889950141264 FDA UDI
FDA Product Code: EMJ FDA UDI
GMDN Term: Periosteal elevator, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Periosteal elevator, reusable

Z21 by Hu-Friedy Mfg Co., Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periosteal elevator, reusable.

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SCANLAN® Instrumentation — SCANLAN INTERNATIONAL INC · Class I
BARRIER PLACEMENT INSTRUMENT — W.H. Holden, Inc. · Class I
ELEVATOR — KLS-Martin L.P. · Class I
HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Hu-Friedy Mfg Co., Llc

Sources (1)

FDA UDI c018ee97-4026-4aea-bc6a-7f1e6dc67784 34 fields · synced Jun 1, 2026