# Pixcell Medical Technologies, Ltd.

- Location (FDA's records): Yokneam Ilit, IL
- FDA decisions: 3 (2018–2024): 3 510(k) clearances
- Names in FDA's records: Pixcell Medical Technologies, Ltd. (2); Pixcell Medical Technologies (1)
- Product codes: GKZ (3)
- 510(k) review time since 2016: median 300 days, against 270 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- Sysmex America, Inc.: 1 (https://510kreport.com/company/sysmex-america)

## Its most-cited devices
- K222148: HemoScreen Hematology Analyzer (2023), cited by 1
- K180020: HemoScreen Hematology Analyzer (2018), cited by 1

## Recent decisions
- K240636: HemoScreen Hematology Analyzer (May 2, 2024)
- K222148: HemoScreen Hematology Analyzer (Aug 16, 2023)
- K180020: HemoScreen Hematology Analyzer (Oct 29, 2018)

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