# Ellman Intl., Inc.

- Location (FDA's records): Hewlett, NY
- FDA decisions: 15 (1996–2001): 15 510(k) clearances
- Product codes: GEI (11), HQR (1), EKZ (1), HEE (1), GEH (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 29 (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
- Erbe USA, Inc.: 2 (https://510kreport.com/company/erbe-usa)

## Firms that cite its devices most
- Senorx, Inc.: 4 (https://510kreport.com/company/senorx)
- Arthrocare Corp.: 3 (https://510kreport.com/company/arthrocare)
- Ellman Int'L, Inc.: 3 (https://510kreport.com/company/ellman-int-l)
- Xomed, Inc.: 2 (https://510kreport.com/company/xomed)
- Ortho Development Corp.: 2 (https://510kreport.com/company/ortho-development)
- Macan Engineering Co.: 1 (https://510kreport.com/company/macan-engineering)
- Ellman International, Inc.: 1 (https://510kreport.com/company/ellman-international)
- Richard Wolf Medical Instruments Corp.: 1 (https://510kreport.com/company/richard-wolf-medical-instruments)

## Its most-cited devices
- K013255: Surgitron 120 Iec (Also Known as Surgitron 4.0 Dual RF (2001), cited by 6
- K003126: Bipolar Trigger-Flex Probe (2001), cited by 5
- K001253: Surgitron Iec II (2000), cited by 4
- K001407: Surgitron Iec II (2000), cited by 3
- K980177: Sugitron Model: Iec (1998), cited by 3
- K980170: Surgitron (1998), cited by 2

## Recent decisions
- K013255: Surgitron 120 Iec (Also Known as Surgitron 4.0 Dual RF (Nov 7, 2001)
- K003126: Bipolar Trigger-Flex Probe (Apr 11, 2001)
- K001986: Surgitron Iec II (Sep 27, 2000)
- K001407: Surgitron Iec II (Jul 24, 2000)
- K001253: Surgitron Iec II (May 26, 2000)
- K992382: Surgitron Radiolase (Oct 14, 1999)
- K990146: Surgitron (Mar 17, 1999)
- K980177: Sugitron Model: Iec (Jul 7, 1998)

Source page: https://510kreport.com/company/ellman-intl