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Alginelle KAL001

by Lascod Spa

Alginelle KAL001 (KAL102) is a Class II device made by Lascod Spa, listed in FDA GUDID since 15 Sep 2017 (UDI-DI 18016200010441), 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 Number18016200010441 UDI-DI Date15 Sep 2017ListedStatusListed 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  • Withdrawn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
Alginelle
Generic name
Alginate dental impression material
Model / Ref / Catalog
KAL001, KAL102
Description
Orange alginate type 1 (450g) CATALOGUE NUMBER: - KAL102 = carton box containing n. 20 bags KAL001
Primary DI / UDI-DI
18016200010441
FDA product code
ELW
GMDN term
Alginate dental impression material
Device class
Class II
Regulation number
872.3660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Alginate dental impression material

Similar devices

Other devices filed under FDA product code ELW (Material, Impression).

Other devices from Lascod Spa

See all devices from Lascod Spa →

Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)