DELL DENT LTD.

FDA Device Registration & Listing · PETACH TIKVAH Central, IL · Registration 9616762

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
9616762
FEI Number
3002806828
Entity Name
DELL DENT LTD.
City/State/Country
PETACH TIKVAH Central, IL
Establishment Address
10 DOV LEVIATAN STREET, PETACH TIKVAH Central 4927177, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dell Dent Ltd. (Owner Number: 9009616)
Owner / Operator Contact Address
10 Dov Leviatan St., --, Petach Tikva, IL-NOTA 4927177, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AIRBRUSH AIRBRUSH AIRBRUSH AIRBRUSH AIRBRUSH

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ELC Scaler, Ultrasonic Dental Class 2 872.4850 2007-12-23
KOJ Airbrush Dental Class 2 872.6080 2007-12-23
ELC Scaler, Ultrasonic Dental Class 2 872.4850 2007-12-20
KOJ Airbrush Dental Class 2 872.6080 1994-02-14
EJR Agent, Polishing, Abrasive, Oral Cavity Dental Class 1 872.6030 2020-08-16

Official Correspondent

Meir Sahar

US Agent Details

Doram Elkayam Business: OBELIS USA LLC Email: regulatory@obelis.us Phone: (513) 7408559

Related Public Records

Same Entity

Dell Dent Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K832443 California Technics, Inc. ULTRASONIC DENTAL PROPHYLAXIS UNIT 1983-09-12
K994299 Bonart Co., Ltd. ART-P3, MODEL P3-1-ART-A1 2000-03-06
K940776 Kreativ, Inc. KREATIV MODEL KV-1 1994-12-21
K121698 Dentsply International, Inc. NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN 2012-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9616762. Last updated year: 2026. Please use registration number 9616762 when referencing this establishment in official correspondence.
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