← Back to catalogue

Platform Neutral Acetabular Insert Trial

FDA UDI

Class I (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name
Platform Neutral Acetabular Insert Trial FDA UDI
Generic Name
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Device Name
Neutral Acetabular Insert Trial, 36mm head, size 62mm FDA UDI
Model / Reference
1226.62.036 FDA UDI
Description
Neutral Acetabular Insert Trial, 36mm head, size 62mm FDA UDI

Identifiers

Primary DI / UDI-DI
00819251029896 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable 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

No

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
Moist Heat or Steam Sterilization FDA UDI

Category: Acetabulum prosthesis trial, prefabricated, reusable

Platform Neutral Acetabular Insert Trial by Total Joint Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabulum prosthesis trial, prefabricated, reusable.

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
Total Joint Orthopedics, Inc.

Sources (1)

  • FDA UDI b3b1da6f-02ed-496e-8ab0-819246a70408 36 fields · synced Jun 1, 2026