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Circon Acmi

Country not established

Devices
10

What Circon Acmi makes

Circon Acmi manufactures endoscopic accessories and therapeutic systems, including the Morris Anti-Splatter Device for endoscopes, insufflators for laparoscopic and hysteroscopic procedures (e.g., LAP 3501, GYN-1500), and electrohydraulic lithotripters with various probe attachments. The company also produces hemorrhoid treatment systems (BICAP Hemorrhoid System BH-10 & BHP-20), ablating forceps (BICAP ABLATING FORCEPS BAF-7), and Bullard intubating laryngoscopes for airway management. Laparoscopes (USA Series) and therapeutic systems like the BICAP II and BICAP III are designed for minimally invasive surgical applications.

The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. These devices are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Circon Acmi have in the registry?

The registry currently lists 10 devices for Circon Acmi. Devices recorded under merged duplicate company entries are counted once.

Which registries list Circon Acmi's devices?

Among its 10 most recently registered devices, Circon Acmi has devices listed in FDA 510(k) (10 devices).

What risk classes do Circon Acmi's devices fall under?

Among its 10 most recently registered devices, the classes recorded for Circon Acmi's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Circon Acmi in the registry?

The most recently registered devices listed for Circon Acmi include MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES, CIRCON ACMI BICAP III THERAPEUTIC SYSTEM, CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20 and BICAP ABLATING FORCEPS BAF-7.

Generated automatically from registry data and not verified by a human reviewer.