Data / Medical devices / Israel / Neteera Technologies Ltd
Neteera Technologies Ltd: FDA-registered device maker in Jerusalem, Israel, 2 510(k) clearances
Neteera Technologies Ltd is registered with the FDA (registration 3014739036) in Jerusalem, Israel. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 9, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014739036
- Address
- Prof. Rakah 3 st., Jerusalem, Israel, 9270403
- Owner or operator
- Neteera Technologies LTD (10077846)
- Roles
- Manufacturer
- First device listed
- October 20, 2022
- Registered through
- 2026
- Brand names listed
- 130H-Plus, Neteera 130H-Plus, Neteera 130H-Plus Vital Sign Monitoring Sensor, Neteera 130H/131H Vital Sign Monitoring Sensor
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Monitor, Breathing Frequency | BZQ | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | DRT | 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 9, 2024 | K231733 | Neteera 130H-Plus Vital Sign Monitoring Sensor | DRT | Substantially Equivalent | Neteera Technologies , Ltd. | accessdata.fda.gov |
| September 28, 2022 | K212143 | Neteera 130H/131H Vital Sign Monitoring Sensor | DRT | Substantially Equivalent | Neteera Technologies , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- All makers of Monitor, Breathing Frequency
Updated February 9, 2024. 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.