# Maxq AL, Ltd.

- Location (FDA's records): Tel Aviv, IL
- FDA decisions: 2 (2018–2020): 2 510(k) clearances
- Names in FDA's records: Maxq AL , Ltd. (1); Maxq-Al , Ltd. (1)
- Product codes: QAS (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 4 (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
- Viz.Al, Inc.: 1 (https://510kreport.com/company/viz-al)

## Firms that cite its devices most
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Zebra Medical Vision, Ltd.: 1 (https://510kreport.com/company/zebra-medical-vision)
- Curacloud Corp.: 1 (https://510kreport.com/company/curacloud)

## Its most-cited devices
- K182177: Accipiolx (2018), cited by 4

## Recent decisions
- K201310: Accipiolx (Aug 7, 2020)
- K182177: Accipiolx (Oct 26, 2018)

Source page: https://510kreport.com/company/maxq-al