# Unimar, Inc.

- Location (FDA's records): Wilton, CT
- FDA decisions: 10 (1981–1994): 10 510(k) clearances
- Product codes: HES (1), EYY (1), HHT (1), HIG (1), HDR (1), LKF (1), HFC (1), HIB (1), MFD (1), HHK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Rocket Medical Plc: 2 (https://510kreport.com/company/rocket-medical)
- Wallach Surgical Devices, Inc.: 1 (https://510kreport.com/company/wallach-surgical-devices)

## Its most-cited devices
- K894264: KDF-2.3 (1989), cited by 1
- K910317: Uni-Sem (TM) (1991), cited by 1
- K854415: Endometrial Pipelle (1986), cited by 1

## Recent decisions
- K932432: Kronner Reinforcing Stylette (Apr 12, 1994)
- K920803: HSG Tray (Oct 19, 1992)
- K910317: Uni-Sem (TM) (May 1, 1991)
- K904473: Kronner Manipujector (Dec 14, 1990)
- K895659: Hui Mini-Flex (Dec 19, 1989)
- K895403: Aspirette Endocervical Aspirator (Nov 29, 1989)
- K894264: KDF-2.3 (Aug 15, 1989)
- K890848: Cervex-Brush (May 11, 1989)

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