← Back to catalogue

Fluted Pin, Square Head, 89mm

FDA UDI

Class I (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name
Fluted Pin, Square Head, 89mm FDA UDI
Generic Name
Joint prosthesis implantation kit, single-use FDA UDI
Device Name
Fluted Pin, Square Head, 89mm FDA UDI
Model / Reference
2707.00.089 FDA UDI
Description
Fluted Pin, Square Head, 89mm FDA UDI

Identifiers

Primary DI / UDI-DI
00819251025829 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Joint prosthesis implantation kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Joint prosthesis implantation kit, single-use

Fluted Pin, Square Head, 89mm by Total Joint Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

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 c2954d3f-e841-4acc-a9f6-80fa3f8d68f1 36 fields · synced Jun 1, 2026