Multiloc

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name: MULTILOC FDA UDI
Generic Name: Bone nail end-cap FDA UDI
Device Name: TI MULTILOC END CAP F/MULTILOC NAIL/15MM EXTENSION-STERILE FDA UDI
Model / Reference: 04.019.015S FDA UDI
Description: TI MULTILOC END CAP F/MULTILOC NAIL/15MM EXTENSION-STERILE FDA UDI

Identifiers

Catalog Number: 04019015S FDA UDI
Primary DI / UDI-DI: 10886982089618 FDA UDI
510(k) Number: K103002 FDA UDI
FDA Product Code: HSB FDA UDI
GMDN Term: Bone nail end-cap FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3020 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone nail end-cap

Multiloc by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Bone nail end-cap.

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PNP Femur — ORTHOPEDIATRICS CORP. · Class II
PNP Femur — ORTHOPEDIATRICS CORP. · Class II
PTN PERITROCHANTERIC NAIL — Biomet Orthopedics, Inc. · Class II

Cleared under the same submission

K103002 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Synthes

Sources (1)

FDA UDI f690b51b-6f00-44d8-8b91-66a7514cd025 36 fields · synced May 30, 2026