# Derata Corp.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 6 (1977–1988): 6 510(k) clearances
- Product codes: KZE (6)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medi-Ject Corp.: 4 (https://510kreport.com/company/medi-ject)

## Its most-cited devices
- K883847: Derata Medi-Jector V (1988), cited by 2
- K864561: Derata Medi-Jector IV (1987), cited by 2

## Recent decisions
- K883847: Derata Medi-Jector V (Oct 31, 1988)
- K864561: Derata Medi-Jector IV (Feb 19, 1987)
- K844244: Derata Medi-Jector Pro (Jul 5, 1985)
- K844111: Derata Medi-Jector Iii (Nov 28, 1984)
- K834044: Medi-Jector II (Mar 6, 1984)
- K772129: Medi-Jector (Dec 8, 1977)

Source page: https://510kreport.com/company/derata