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Dr. Joseph E. Grasso, D.D.S.

Country not established

Devices
3

What Dr. Joseph E. Grasso, D.D.S. makes

The company produces mechanical coupling devices designed to securely and rapidly attach dental prostheses, including removable dentures and partials. These devices include quick-release mechanisms for ease of use by patients. The portfolio includes standalone coupling attachments and systems that integrate with existing prostheses.

The devices are classified under FDA regulations as Class I and Class II, with some requiring 510(k) clearance. They are listed in the FDA’s 510(k) premarket notification database. The manufacturer operates from the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

Frequently asked questions

How many devices does Dr. Joseph E. Grasso, D.D.S. have in the registry?

The registry currently lists 3 devices for Dr. Joseph E. Grasso, D.D.S.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dr. Joseph E. Grasso, D.D.S.'s devices?

Among its 3 most recently registered devices, Dr. Joseph E. Grasso, D.D.S. has devices listed in FDA 510(k) (3 devices).

What risk classes do Dr. Joseph E. Grasso, D.D.S.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Dr. Joseph E. Grasso, D.D.S.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Dr. Joseph E. Grasso, D.D.S. in the registry?

The most recently registered devices listed for Dr. Joseph E. Grasso, D.D.S. include COUPLING DEVICE FOR DENTAL PROSTHESIS, QUICK COUPLING DEVICE FOR DENTAL PROSTHESES and DEVICE FOR PROVIDING QUICK COUPLING FOR DENTAL PROSTHESES.

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