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Sklar® 96-5391

by Sklar Corporation

Sklar® 96-5391 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 23 Oct 2018 (UDI-DI 50649111110649), 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 Number50649111110649 UDI-DI Date23 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  • Withdrawn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
General-purpose surgical scissors, single-use
Model / reference
96-5391
Primary DI / UDI-DI
50649111110649
FDA product code
LRW
GMDN term
General-purpose surgical scissors, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose surgical scissors, single-use

Similar devices

Other devices filed under FDA product code LRW (SCISSORS, GENERAL, SURGICAL).

Other devices from Sklar Corporation

See all devices from Sklar Corporation →

Properties

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