Skip to content

K-Wire Ø2.4mm x 280mm - Blunt Tip 202-280

by McNicoll Chirurgical Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07540161800208 UDI-DI Date27 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
K-Wire Ø2.4mm x 280mm - Blunt Tip
Generic Name
Orthopaedic guidewire, single-use
Model / Reference
202-280
Primary DI / UDI-DI
07540161800208
510(k) Number
FDA Product Code
LXH
GMDN Term
Orthopaedic guidewire, single-use
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Guidewire Diameter — 2.4 Millimeter
Guidewire Length — 280 Millimeter

Related devices

Cleared under the same submission (K253611)

Show all (12)

Other devices from McNicoll Chirurgical Inc.

See all devices from McNicoll Chirurgical Inc. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No