Data / Medical devices / Israel / Dell Dent Ltd.
Dell Dent Ltd.: FDA-registered device maker in PETACH TIKVAH Central, Israel, 6 510(k) clearances
Dell Dent Ltd. is registered with the FDA (registration 9616762) in PETACH TIKVAH Central, Israel. It lists 3 device types. The FDA files 6 510(k) clearances under its listings, the newest dated February 19, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9616762
- FEI number
- 3002806828
- Address
- 10 Dov Leviatan Street, PETACH TIKVAH Central, Israel, 4927177
- Owner or operator
- Dell Dent Ltd. (9009616)
- Roles
- Manufacturer
- First device listed
- February 14, 1994
- Registered through
- 2026
- Brand names listed
- AIRBRUSH
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Agent, Polishing, Abrasive, Oral Cavity | EJR | 1 | Manufacturer | accessdata.fda.gov |
| Airbrush | KOJ | 2 | Manufacturer | accessdata.fda.gov |
| Scaler, Ultrasonic | ELC | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 19, 2002 | K014252 | JETSTREAM | KOJ | Substantially Equivalent | Deldent , Ltd. | accessdata.fda.gov |
| February 19, 2002 | K014249 | JETPOLISHER | KOJ | Substantially Equivalent | Deldent , Ltd. | accessdata.fda.gov |
| January 29, 2002 | K014245 | JETSONIC 2000 | KOJ | Substantially Equivalent | Deldent , Ltd. | accessdata.fda.gov |
| January 24, 2002 | K014238 | DELSONIC 2000 | ELC | Substantially Equivalent | Deldent , Ltd. | accessdata.fda.gov |
| January 10, 2002 | K013969 | MINIBLASTER | KOJ | Substantially Equivalent | Deldent , Ltd. | accessdata.fda.gov |
| June 5, 2001 | K011179 | DELDENT ULTRASONIC INSERTS | ELC | Substantially Equivalent | Deldent , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Airbrush
- All makers of Scaler, Ultrasonic
- All makers of Agent, Polishing, Abrasive, Oral Cavity
Updated February 19, 2002. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.