Identity

Trade Name
DynaFORCE™ FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
DynaFORCE 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™ MotoCLIP™ Max Inserter, 12mm FDA UDI
Description
DynaFORCE 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
245104 FDA UDI
Primary DI / UDI-DI
00815432024131 FDA UDI
510(k) Number
K142727 FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bone staple, non-adjustable

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

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

Cleared under the same submission

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 dfc78f21-66a1-4b04-a53c-4e132a37fde1 37 fields · synced May 31, 2026