← Back to catalogue

Leith Medical Lapidus Plating System

FDA UDI

Class II (US FDA UDI)

by Leith Medical LLC

Identity

Trade Name
Leith Medical Lapidus Plating System FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
0° Lapidus Plate Left 0mm Step Down FDA UDI
Model / Reference
0100-0000-L FDA UDI
Description
0° Lapidus Plate Left 0mm Step Down FDA UDI

Identifiers

Catalog Number
01000000L FDA UDI
Primary DI / UDI-DI
B95301000000L0 FDA UDI
510(k) Number
K200062 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Angle — 0 degree FDA UDI
Width — 0 Millimeter FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Leith Medical Lapidus Plating System by Leith Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Leith Medical LLC

Sources (1)

  • FDA UDI ff5badc2-e32a-4b66-b0f2-501081067807 37 fields · synced Jun 6, 2026