Skip to content

Sklar Instruments 96-2659

by Sklar Corporation

Sklar Instruments 96-2659 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 21 Jan 2025 (UDI-DI 10649111077661), 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 Number10649111077661 UDI-DI Date21 Jan 2025ListedStatusListed 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  • Withdrawn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 Instruments
Generic name
Suturing needle holder, single-use
Model / reference
96-2659
Primary DI / UDI-DI
10649111077661
FDA product code
HXK
GMDN term
Suturing needle holder, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Suturing needle holder, single-use

Other devices from Sklar Corporation

See all devices from Sklar Corporation →

Properties

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