Skip to content

Carticept Medical, Inc.

United StatesFDA applicant, unverified

Devices
9

What Carticept Medical, Inc. makes

Carticept Medical, Inc. manufactures the Navigator Delivery System, including the NAV-010 model and the Navigator Aesthetic Delivery System, which are designed for controlled substance administration in medical procedures.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Company details

DUNS number
619025609
Phone
770-754-3800

Frequently asked questions

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

The registry currently lists 9 devices for Carticept Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

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

Among its 9 most recently registered devices, Carticept Medical, Inc. has devices listed in FDA 510(k) (6 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 9 most recently registered devices, the classes recorded for Carticept Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Carticept Medical, Inc. include Navigator Aesthetic Delivery System NAV-013, Navigator Aesthetic Delivery System NAV-015, Navigator Aesthetic Delivery System NAV-038 and NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS).

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