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Sklar® 42-4245

by Sklar Corporation

Sklar® 42-4245 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 4 Oct 2018 (UDI-DI 10649111404412), 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 Number10649111404412 UDI-DI Date4 Oct 2018ListedStatusListed 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  • Withdrawn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
Sklar®
Generic name
Orthopaedic joint/limb rongeur
Model / reference
42-4245
Primary DI / UDI-DI
10649111404412
FDA product code
HTX
GMDN term
Orthopaedic joint/limb rongeur
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic joint/limb rongeur

Similar devices in this category

Other devices filed under Orthopaedic joint/limb rongeur.

Other devices from Sklar Corporation

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)