DynaFORCE™

FDA UDI

Class II (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name: DynaFORCE™ FDA UDI
Generic Name: Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name: DynaFORCE MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis FDA UDI
Model / Reference: DynaFORCE 18mm Clip Prep Kit FDA UDI
Description: DynaFORCE MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis FDA UDI

Identifiers

Catalog Number: 7100-1800 FDA UDI
Primary DI / UDI-DI: 00815432027538 FDA UDI
FDA Product Code: JDR FDA UDI
HRS FDA UDI
HWC FDA UDI
GMDN Term: Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical drill guide, reusable Orthopaedic inorganic implant inserter/extractor, reusable Surgical tamp, reusable Surgical drill guide, single-use

DynaFORCE™ by Crossroads Extremity Systems Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical tamp, single-use.

Mallet — DR.FRIGZ INTERNATIONAL(PVT)LTD, · Class I
8-Gauge Bone Access Needle and Tamp — Si-Bone Inc. · Class I
DynaFORCE™ — CROSSROADS EXTREMITY SYSTEMS LLC · Class II
DynaFORCE™ — CROSSROADS EXTREMITY SYSTEMS LLC · Class II
DynaFORCE™ — CROSSROADS EXTREMITY SYSTEMS LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Crossroads Extremity Systems Llc

Sources (1)

FDA UDI 3190f7aa-4b0c-4c0d-8255-cc7054f414d4 35 fields · synced May 30, 2026