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Prowess, Inc.

United StatesFDA applicant, unverified FDA FEI 2939248

Prowess, Inc. is a medical device manufacturer, with 37 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.

Devices
37
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 28
  • FDA 510(k) 9

A device listed in two registries counts in both.

Device classes
  • FDA Class II 37
Identifiers
  • FDA FEI 2939248
  • DUNS 002162728

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Prowess, Inc. makes

Prowess, Inc. manufactures radiation therapy treatment record and verification systems, including treatment planning software and on-treatment verification tools. Their portfolio includes systems like the Panther TPS for treatment planning, Panther OIS for real-time verification, and specialized models such as Panther Stereotactic and PUMA for targeted radiation delivery.

These devices are classified as Class II under FDA regulations and are listed via 510(k) premarket notifications and the FDA’s Unique Device Identifier (UDI) system.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue37

Newest first, rows 1-37 of 37

Search and filter all 37 devices
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  • Panther TPS 6.4

    Listed Registry: GUDID Class:II
  • Panther OIS 3.3

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 6.2

    Listed Registry: GUDID Class:II
  • Panther TPS 6.1

    Listed Registry: GUDID Class:II
  • Panther OIS 3.31

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 6.21

    Listed Registry: GUDID Class:II
  • Panther OIS 3.4

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther OIS 3.5

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 6.3

    Listed Registry: GUDID Class:II
  • Panther TPS 6.0

    Listed Registry: GUDID Class:II
  • Panther Brachy version 5.0

    Withdrawn Registry: GUDID Class:II
  • Panther OIS 3.12

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther OIS v3.0

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 5.8

    Withdrawn Registry: GUDID Class:II
  • Panther OIS 3.11

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 5.81

    Listed Registry: GUDID Class:II
  • Panther Brachy version 5.0

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther OIS|R&V 2.2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 5.7

    Withdrawn Registry: GUDID Class:II
  • Panther TPS v5.61

    Withdrawn Registry: GUDID Class:II
  • Panther OIS|R&V v2.31

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 5.7

    Withdrawn Registry: GUDID Class:II
  • Panther TPS 5.7

    Withdrawn Registry: GUDID Class:II
  • Panther OIS 3.2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS v5.6

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther OIS 3.1

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther TPS 5.9

    Listed Registry: GUDID Class:II
  • Panther TPS version 5.51

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Panther Stereotactic Ref K193459

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Panther Ois/R & V Model Version 2.0 Ref K122616

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Puma Model Version 1.0 Ref K100801

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Prowess Panther Proarc, Model Version 5.0 Ref K101076

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Panther OIS Ref K211760

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Panther StereoSeed Ref K143514

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Prowess Ref K032456

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Panther TPS Ref K231825

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Panther Realart, Model 4.7 Ref K083502

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-37 of 37

Company details

FDA FEI number
2939248
DUNS number
002162728
Address
5129 Commercial Circle, Concord, CA, 94520
Phone
(925) 405-6556

Frequently asked questions

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

The registry currently lists 37 devices for Prowess, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Prowess, Inc.'s devices?

Among its 37 most recently registered devices, Prowess, Inc. has devices listed in FDA 510(k) (9 devices) and FDA GUDID (28 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 37 most recently registered devices, the classes recorded for Prowess, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Prowess, Inc. include Panther TPS 6.4, Panther OIS 3.3, Panther TPS 6.2 and Panther TPS 6.1.

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