Data / Medical devices / Israel / Noga Medical Products Ltd.
Noga Medical Products Ltd.: FDA-registered device maker in SHLOMI Northern, Israel, 1 510(k) clearance
Noga Medical Products Ltd. is registered with the FDA (registration 3021630667) in SHLOMI Northern, Israel. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 14, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021630667
- Address
- Hakriya 1, SHLOMI Northern, Israel, 2283200
- Owner or operator
- NOGA MEDICAL PRODUCTS LTD. (10086141)
- Roles
- Manufacturer
- First device listed
- October 18, 2022
- Registered through
- 2026
- Brand names listed
- Axis Implant ø3.30 L10mm, Axis Implant ø3.30 L11.50mm, Axis Implant ø3.30 L13mm, Axis Implant ø3.30 L16mm, Axis Implant ø3.75 L10mm, Axis Implant ø3.75 L11.50mm, Axis Implant ø3.75 L13mm, Axis Implant ø3.75 L16mm and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Instruments, Dental Hand | DZN | 1 | 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 |
|---|---|---|---|---|---|---|
| May 14, 2015 | K143326 | T.A.G. Dental Implant System | DZE | Substantially Equivalent | T.A.G. Medical Products Corporation, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Instruments, Dental Hand
- All makers of Drill, Dental, Intraoral
Updated May 14, 2015. 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.