← Back to catalogue

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 inorganic implant inserter/extractor, reusable FDA UDI
Device Name
MEMO STAPLE 10MM & 12MM EXPANDER FDA UDI
Model / Reference
OS361007 FDA UDI
Description
MEMO STAPLE 10MM & 12MM EXPANDER FDA UDI

Identifiers

Catalog Number
OS361007 FDA UDI
Primary DI / UDI-DI
05055662929270 FDA UDI
510(k) Number
K111678 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, reusable

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 inorganic implant inserter/extractor, reusable.

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 4af86d21-4be2-48fb-966a-3e4ba64f57d1 36 fields · synced Jun 8, 2026