PediNail Intramedullary Platform

FDA UDI

Class I (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name: PediNail Intramedullary Platform FDA UDI
Generic Name: Screw-extraction orthopaedic reamer, reusable FDA UDI
Device Name: 12.5MM MODULAR REAMER HEAD FDA UDI
Model / Reference: 01-1500-125 FDA UDI
Description: 12.5MM MODULAR REAMER HEAD FDA UDI

Identifiers

Catalog Number: 01-1500-125 FDA UDI
Primary DI / UDI-DI: 00841132150085 FDA UDI
FDA Product Code: HTO FDA UDI
GMDN Term: Screw-extraction orthopaedic reamer, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Screw-extraction orthopaedic reamer, reusable

PediNail Intramedullary Platform by Orthopediatrics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Orthopediatrics Corp.

Sources (1)

FDA UDI 553f4803-a1c4-472f-bd7e-e8e4ca7c89d4 35 fields · synced Jun 6, 2026