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Hintermann Series

FDA UDI

Class I (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Hintermann Series FDA UDI
Generic Name
Orthopaedic intraoperative positioning pin, reusable FDA UDI
Device Name
Hintermann Series 105mm Smooth Pin, Non-Threaded FDA UDI
Model / Reference
HT-39870 FDA UDI
Description
Hintermann Series 105mm Smooth Pin, Non-Threaded FDA UDI

Identifiers

Primary DI / UDI-DI
00841731134783 FDA UDI
510(k) Number
K240475 FDA UDI
FDA Product Code
HXI FDA UDI
GMDN Term
Orthopaedic intraoperative positioning pin, 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: Orthopaedic intraoperative positioning pin, reusable

Hintermann Series by Vilex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic intraoperative positioning pin, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI c0a98400-3585-48aa-a179-e7c2d9c0f032 36 fields · synced May 30, 2026