Skip to content

Corbin Clinical Resources

Country not established FDA

Devices
3
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

Catalogue3

Newest first, rows 1-3 of 3

Company details

Phone
18882721001(from company website)

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Corbin Clinical Resources, LLC Cumberland, MD · US FEI 3012975098

From the company website

Read 18 Oct 2026

The PrecisionPoint™ system enables transperineal prostate biopsy with targeted template sampling and low infection rates. Designed for efficient, office-based procedures.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Corbin Clinical Resources have in the registry?

The registry currently lists 3 devices for Corbin Clinical Resources. Devices recorded under merged duplicate company entries are counted once.

Which registries list Corbin Clinical Resources's devices?

Among its 3 most recently registered devices, Corbin Clinical Resources has devices listed in FDA GUDID (3 devices).

What risk classes do Corbin Clinical Resources's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Corbin Clinical Resources's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Corbin Clinical Resources in the registry?

The most recently registered devices listed for Corbin Clinical Resources include PrecisionPoint P1003 and Perineologic 1.

Which FDA establishments are linked to Corbin Clinical Resources?

1 FDA establishment is linked to Corbin Clinical Resources in the registry; they are listed on the company page.

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