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PunchTac Shuttle Wire Loop DM-4830

by Dunamis Medical LLC

PunchTac Shuttle Wire Loop DM-4830 is a Class I device made by Dunamis Medical LLC, listed in FDA GUDID since 17 Aug 2023 (UDI-DI 00854629006345), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854629006345 UDI-DI Date17 Aug 2023ListedStatusListed 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  • Withdrawn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
PunchTac Shuttle Wire Loop
Generic name
Orthopaedic bone wire
Model / Ref / Catalog
DM-4830
Primary DI / UDI-DI
00854629006345
FDA product code
HWQ
GMDN term
Orthopaedic bone wire
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic bone wire

Similar devices in this category

Other devices filed under Orthopaedic bone wire.

Other devices from Dunamis Medical LLC

See all devices from Dunamis Medical LLC →

Properties

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