Skip to content

Pulp Canal Sealer 24873

by Ormco Corporation

Pulp Canal Sealer 24873 is a Class II device made by Ormco Corporation, cleared under FDA 510(k) K152956 on 6 May 2016 and listed in FDA GUDID since 8 Sep 2016 (UDI-DI 00889989074154), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K152956

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889989074154 UDI-DI Date8 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK152956 Date6 May 2016DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K152956 decided 6 May 2016 Active
  • FDA GUDID UDI-DI 00889989074154 listed 8 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K152956
  2. Listed FDA GUDID 00889989074154

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Pulp Canal Sealer
Generic name
Hygroscopic dental cement
Model / reference
24873
Primary DI / UDI-DI
00889989074154
510(k) Number
FDA product code
KIF
GMDN term
Hygroscopic dental cement
Device class
Class II
Regulation number
872.3820
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 16 Milliliter

Related devices

Category: Endodontic filling/sealing material

Cleared under the same submission (K152956)

Other devices from Ormco Corporation

See all devices from Ormco Corporation →

Properties

  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)