# Neteera Technologies, Ltd.

- Location (FDA's records): Jerusalem, IL
- FDA decisions: 2 (2022–2024): 2 510(k) clearances
- Product codes: DRT (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Xandar Kardian, Inc.: 1 (https://510kreport.com/company/xandar-kardian)

## Its most-cited devices
- K212143: Neteera 130H/131H Vital Sign Monitoring Sensor (2022), cited by 1

## Recent decisions
- K231733: Neteera 130H-Plus Vital Sign Monitoring Sensor (Feb 9, 2024)
- K212143: Neteera 130H/131H Vital Sign Monitoring Sensor (Sep 28, 2022)

Source page: https://510kreport.com/company/neteera-technologies