← Back to catalogue

Neo Medical Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
Neo Medical Pedicle Screw System FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
1.5mm K-wire (1x2) FDA UDI
Model / Reference
KW-00-00-01 FDA UDI
Description
1.5mm K-wire (1x2) FDA UDI

Identifiers

Primary DI / UDI-DI
07640177820457 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

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
Outer Diameter — 1.5 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

Neo Medical Pedicle Screw System by Neo Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

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
Neo Medical Inc.

Sources (1)

  • FDA UDI f9df8d9a-eb36-49e5-85a5-31f1b3f4482e 34 fields · synced Jun 1, 2026