Elastic Impression Material

FDA 510(k) K241924 · Beijing Okvd Biological Technology , Ltd.

Substantially Equivalent

510(k) numberK241924

Submission

Device name
Elastic Impression Material
Applicant
Beijing Okvd Biological Technology , Ltd.
Beijing, CN
Received
July 1, 2024
Decision date
December 27, 2024
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ELW – Material, Impression
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3660
Specialty
Dental

Other 510(k)s with product code ELW

510(k)DeviceApplicantDecision
K254112Dia-X Sil BiteELW · Traditional DiaDent Group International03/19/2026SE
K253501Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium Regular Set -…ELW · Traditional Vigodent Indústria E Comercio Ltda10/31/2025SE
K250969Jet Bite; Jet Blue Bite Fast; Jet Blue Bite SuperfastELW · Abbreviated Dent4you AG06/27/2025SE
K242360Speedex Light Body; Speedex Medium; Speedex Putty; Speedex Putty Soft; Speedex Universal…ELW · Traditional Dent4you AG11/15/2024SE
K233954Chemi-SiL (HB, MB, LB, LBS); Chemi-SiL Bite-BluELW · Traditional B&E Korea Co., Ltd.02/13/2024SE
K223892DentMix VPS Impression MaterialELW · Traditional Innovative Product Brands, Inc.04/27/2023SE
K213175No Stress ImpressELW · Traditional No Stress Impress, LLC01/19/2023SE
K214086Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite…ELW · Traditional Genoss Co., Ltd.12/15/2022SE
K222741DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular…ELW · Traditional Hdi, Inc.11/07/2022SE
K213244Accusil Dental Impression Materials (Accusil Light Body Regular and Fast Set, Accusil…ELW · Traditional Prevest Denpro Limited09/09/2022SE

Questions and answers

When was Elastic Impression Material cleared by the FDA?

Elastic Impression Material (K241924) received a 510(k) decision of Substantially Equivalent on December 27, 2024, 179 days after the submission was received.

What is the product code of K241924?

The FDA product code is ELW – Material, Impression, a Class II (moderate risk) device regulated under 21 CFR 872.3660.