# Circon Acmi

- Location (FDA's records): Stamford, CT
- FDA decisions: 10 (1988–2002): 10 510(k) clearances
- Product codes: KNS (4), GCJ (1), CCW (1), HIF (1), ODC (1), HIG (1), FFK (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Surgical Image Laboratories, Inc.: 2 (https://510kreport.com/company/surgical-image-laboratories)
- Richard Wolf Medical Instruments Corp.: 1 (https://510kreport.com/company/richard-wolf-medical-instruments)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)

## Firms that cite its devices most
- Acmi Corporation: 1 (https://510kreport.com/company/acmi)
- Seedling Enterprises., LLC: 1 (https://510kreport.com/company/seedling-enterprises)
- Novadaq Technologies, Inc.: 1 (https://510kreport.com/company/novadaq-technologies)
- Medisiss: 1 (https://510kreport.com/company/medisiss)
- Mauna Kea Technologies: 1 (https://510kreport.com/company/mauna-kea-technologies)

## Its most-cited devices
- K013165: Usa Series Laparoscopes (2002), cited by 3
- K884306: Bicap Ablating Forceps Baf-7 (1989), cited by 2

## Recent decisions
- K013165: Usa Series Laparoscopes (Jan 18, 2002)
- K980492: Aeh-3 Electrohydraulic Lithotripter and Probes (E-1F, E-3F, E-5F, and E-9F) (Nov 17, 1998)
- K905705: Lap 3501 High Flow Insufflator (Feb 28, 1991)
- K905706: Gyn-1500 Hysteroscopic Inufflator (Feb 28, 1991)
- K884097: Morris Anti-Splatter Device for Endoscopes (Apr 17, 1989)
- K884025: Circon Acmi Bicap II Therapeutic System BC-200 (Mar 3, 1989)
- K884254: Circon Acmi Bicap Iii Therapeutic System (Jan 11, 1989)
- K884252: Circon Acmi Bicap Hemorrhoid System BH-10 & BHP-20 (Jan 10, 1989)

Source page: https://510kreport.com/company/circon-acmi