Lcp

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name: LCP FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name: PEDIATRIC LCP(TM) HIP PLATE 3.5MM 100° FDA UDI
Model / Reference: 02.108.310 FDA UDI
Description: PEDIATRIC LCP(TM) HIP PLATE 3.5MM 100° FDA UDI

Identifiers

Catalog Number: 02108310 FDA UDI
Primary DI / UDI-DI: 10886982029652 FDA UDI
510(k) Number: K062872 FDA UDI
K072095 FDA UDI
K112085 FDA UDI
FDA Product Code: HRS FDA UDI
HWC FDA UDI
JDS FDA UDI
GMDN Term: Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

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

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Also classified as Orthopaedic fixation plate, non-bioabsorbable.

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Cleared under the same submission

K062872 also covers:

K072095 also covers:

K112085 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 420e3a15-06d8-4602-9fce-501afc5937ea 36 fields · synced May 30, 2026