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Ortho Solutions Extremity Fixation Implants For Osteosysnthesis

FDA UDI

Class II (US FDA UDI)

by Ortho Solutions Holdings Limited

Identity

Trade Name
ORTHO SOLUTIONS EXTREMITY FIXATION IMPLANTS FOR OSTEOSYSNTHESIS FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
FOS GUIDE WIRE 0.8MM X 80MM TROCAR TIP FDA UDI
Model / Reference
OS292080H FDA UDI
Description
FOS GUIDE WIRE 0.8MM X 80MM TROCAR TIP FDA UDI

Identifiers

Catalog Number
OS292080H FDA UDI
Primary DI / UDI-DI
05055662935233 FDA UDI
510(k) Number
K111678 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic bone wire 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Orthopaedic bone wire

Ortho Solutions Extremity Fixation Implants For Osteosysnthesis by Ortho Solutions Holdings Limited — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Orthopaedic bone wire.

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 426128f1-5b1d-4e64-8c0f-29d05fd39add 35 fields · synced May 30, 2026