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PediLoc Fragment System

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name
PediLoc Fragment System FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
2.7mm Cortical Screw, T10, 20mm FDA UDI
Model / Reference
00-1005-2526 FDA UDI
Description
2.7mm Cortical Screw, T10, 20mm FDA UDI

Identifiers

Catalog Number
00-1005-2526 FDA UDI
Primary DI / UDI-DI
00841132112397 FDA UDI
510(k) Number
K140431 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bone screw (non-sliding)

PediLoc Fragment System by Orthopediatrics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04409dd1-c4a3-498e-bec9-2ff24aa71af7 36 fields · synced May 30, 2026