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6056

by Medtronic, Inc. 2 variants

6056 is a Class I device made by Medtronic, Inc., listed in FDA GUDID since 13 Jan 2019 (UDI-DI 00763000059330), 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 Number00763000059330 UDI-DI Date13 Jan 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  • Withdrawn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

Generic name
Torque manipulation device
Model / reference
6056
Primary DI / UDI-DI
00763000059330
FDA product code
DWS
GMDN term
Torque manipulation device
Device class
Class I
Regulation number
870.4500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Torque manipulation device

Similar devices

Other devices filed under FDA product code DWS (INSTRUMENTS, SURGICAL, CARDIOVASCULAR).

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

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