← Back to catalogue

Ortho Solutions Trauma Plates For Osteosysnthesis

FDA UDI

Class II (US FDA UDI)

by Ortho Solutions Holdings Limited

Identity

Trade Name
ORTHO SOLUTIONS TRAUMA PLATES FOR OSTEOSYSNTHESIS FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
2.7MM A.C.P. PLATE 10 HOLE FDA UDI
Model / Reference
OS471010 FDA UDI
Description
2.7MM A.C.P. PLATE 10 HOLE FDA UDI

Identifiers

Catalog Number
OS471010 FDA UDI
Primary DI / UDI-DI
05055662901030 FDA UDI
510(k) Number
K120360 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

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 fixation plate, non-bioabsorbable

Ortho Solutions Trauma Plates For Osteosysnthesis by Ortho Solutions Holdings Limited — 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

Sources (1)

  • FDA UDI d515eb3d-791e-4939-8e70-77551ac87e1f 36 fields · synced May 30, 2026