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DynaFORCE™ DynaFORCE 15mm Clip Prep Kit

by Crossroads Extremity Systems LLC

DynaFORCE™ DynaFORCE 15mm Clip Prep Kit (7100-1500) is a Class II device made by Crossroads Extremity Systems LLC, listed in FDA GUDID since 11 Dec 2019 (UDI-DI 00815432027521), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00815432027521 UDI-DI Date11 Dec 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
DynaFORCE™
Generic name
Surgical drill guide, reusable
Model / Ref / Catalog
DynaFORCE 15mm Clip Prep Kit, 7100-1500
Primary DI / UDI-DI
00815432027521
FDA product code
JDR, HRS, HWC
GMDN term
Surgical drill guide, reusable
Device class
Class II
Regulation number
888.3030, 888.3040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical drill guide, reusableOrthopaedic inorganic implant inserter/extractor, reusableSurgical tamp, reusableSurgical drill guide, single-use

Other devices from Crossroads Extremity Systems LLC

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)