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OrthoSolutions 'System26' Bone Screws

FDA UDI

Class I (US FDA UDI)

by Ortho Solutions Holdings Limited

Identity

Trade Name
OrthoSolutions 'System26' Bone Screws FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
DEPTH GAUGE PROBE FOR 2.0-4.0MM SCREWS FDA UDI
Model / Reference
OS900071-NS FDA UDI
Description
DEPTH GAUGE PROBE FOR 2.0-4.0MM SCREWS FDA UDI

Identifiers

Catalog Number
OS900071-NS FDA UDI
Primary DI / UDI-DI
05055662956610 FDA UDI
510(k) Number
K163489 FDA UDI
FDA Product Code
HTJ FDA UDI
GMDN Term
Surgical depth gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4300 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: Surgical depth gauge, reusable

OrthoSolutions 'System26' Bone Screws by Ortho Solutions Holdings Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical depth gauge, reusable.

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 734742f5-d696-4810-ac51-055723ab0b01 36 fields · synced May 30, 2026