Pediatric Nailing Platform | Tibia

FDA UDI

Class I (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name: Pediatric Nailing Platform | Tibia FDA UDI
Generic Name: Screw-extraction orthopaedic reamer, reusable FDA UDI
Device Name: REAMER HEAD, Ø10.0 MM FDA UDI
Model / Reference: 01-1500-100 FDA UDI
Description: REAMER HEAD, Ø10.0 MM FDA UDI

Identifiers

Catalog Number: 01-1500-100 FDA UDI
Primary DI / UDI-DI: 00841132123508 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

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Screw-extraction orthopaedic reamer, reusable

Pediatric Nailing Platform | Tibia 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 9f6c4da0-9a89-4c27-be42-646eef0b5a44 35 fields · synced Jun 8, 2026