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Sklar 24-1022

by Sklar Corporation

Sklar 24-1022 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 31 May 2019 (UDI-DI 30649111319123), 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 Number30649111319123 UDI-DI Date31 May 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  • Withdrawn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

Trade name
Sklar
Generic name
Scalp wound clip
Model / reference
24-1022
Primary DI / UDI-DI
30649111319123
FDA product code
FZQ
GMDN term
Scalp wound clip
Device class
Class I
Regulation number
878.4320
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Scalp wound clip

Similar devices

Other devices filed under FDA product code FZQ (CLIP, REMOVABLE (SKIN)).

Other devices from Sklar Corporation

See all devices from Sklar Corporation →

Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)