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Dukal 15100

by Dukal LLC

Dukal 15100 is a Class I device made by Dukal LLC, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 10665973006441), 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 Number10665973006441 UDI-DI Date6 Dec 2022ListedStatusListed 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  • Withdrawn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
Dukal
Generic name
Suture removal kit
Model / Ref / Catalog
15100
Primary DI / UDI-DI
10665973006441
FDA product code
MCZ
GMDN term
Suture removal kit
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suture removal kit

Other devices from Dukal LLC

See all devices from Dukal LLC →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (9, all answered No)