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Paxeon Origin

FDA UDI

Class II (US FDA UDI)

by Paxeon Reconstruction Llc

Identity

Trade Name
Paxeon Origin FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Model / Reference
Origin Stem Lateral Offset Collared Size 14 FDA UDI

Identifiers

Catalog Number
PR111-18-1403 FDA UDI
Primary DI / UDI-DI
08177570205028 FDA UDI
510(k) Number
K161155 FDA UDI
FDA Product Code
KWZ FDA UDI
MEH FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3310 FDA UDI
888.3353 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

Category: Coated femoral stem prosthesis, modular

Paxeon Origin by Paxeon Reconstruction Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

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 aa100329-71ae-47d0-93f2-990d2210bf46 34 fields · synced Jun 1, 2026