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Opticon Medical, Inc.

Also registered as Opticon Medical

United StatesFDA applicant, unverified

Devices
8

What Opticon Medical, Inc. makes

Opticon Medical, Inc. manufactures medical devices for airway management, urinary drainage, and regional anesthesia. Their products include the Weingarten capnographic intubation stylette for airway confirmation, direct male urinary catheters for continuous drainage, and urinary catheters with adapters for compatibility with drainage systems. They also supply hemostasis valve and tubing sets, epidural catheters for spinal anesthesia, and the Loper celiac plexus block catheter kit for nerve block procedures.

The company’s devices are classified under FDA regulations as Class I and Class II, with some products requiring 510(k) clearance. These products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

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

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

How many devices does Opticon Medical, Inc. have in the registry?

The registry currently lists 8 devices for Opticon Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Opticon Medical, Inc.'s devices?

Among its 8 most recently registered devices, Opticon Medical, Inc. has devices listed in FDA 510(k) (8 devices).

What risk classes do Opticon Medical, Inc.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Opticon Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Opticon Medical, Inc. in the registry?

The most recently registered devices listed for Opticon Medical, Inc. include WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE, OPTION-VM URINARY CATHETER/ADPATER, MODELS MV39016, MVA39016, OPTICON DIRECT MALE URINARY CATHETER FOR CONTINUOUS DRAINAGE and OPTION-VF URINARY CATHETER, FV14218.

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