← Back to catalogue

Axs

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
AXS FDA UDI
Generic Name
Craniofacial bone screw, non-bioabsorbable FDA UDI
Device Name
BONE SCREW, AXS, SELF-TAPPING FDA UDI
Model / Reference
31-17005 FDA UDI
Description
BONE SCREW, AXS, SELF-TAPPING FDA UDI

Identifiers

Catalog Number
31-17005 FDA UDI
Primary DI / UDI-DI
07613327358674 FDA UDI
510(k) Number
K172572 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Craniofacial bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 5.0 Millimeter FDA UDI

Category: Craniofacial bone screw, non-bioabsorbable

Axs by Stryker Leibinger — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial bone screw, 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

Manufacturer
Stryker Leibinger

Sources (1)

  • FDA UDI 16c89a60-d0d9-4ff2-9cde-c90c503df052 36 fields · synced May 30, 2026