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Extended Trocar Tip Reduction Tool

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
Extended Trocar Tip Reduction Tool FDA UDI
Generic Name
Orthopaedic bone-reduction tool FDA UDI
Device Name
Extended Trocar Tip Reduction Tool FDA UDI
Model / Reference
322-0001 FDA UDI
Description
Extended Trocar Tip Reduction Tool FDA UDI

Identifiers

Catalog Number
322-0001 FDA UDI
Primary DI / UDI-DI
00810074306447 FDA UDI
510(k) Number
K170021 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Orthopaedic bone-reduction tool 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

Yes

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

Yes

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 bone-reduction tool

Extended Trocar Tip Reduction Tool by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone-reduction tool.

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 6a0b2b4d-69de-41d9-aa0f-31f5f33fdfeb 36 fields · synced Jun 8, 2026