PROSCIA, INC.

FDA Device Registration & Listing · Philadelphia, PA, US · Registration 3025774973

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3025774973
FEI Number
3025774973
Entity Name
PROSCIA, INC.
City/State/Country
Philadelphia, PA, US
Establishment Address
1700 Market St Fl 24, Philadelphia, PA 19103, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Proscia, Inc. (Owner Number: 10060244)
Owner / Operator Contact Address
1700 Market Street, 24th Floor, Philadelphia, PA 19103, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230839
PMA Number
N/A

All Registered Proprietary Names

Concentriq Dx Concentriq AP-Dx Concentriq AP-Dx-US

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PSY Whole Slide Imaging System Pathology Class 2 864.3700 2024-03-27
QKQ Digital Pathology Image Viewing And Management Software Pathology Class 2 864.3700 2024-03-27

Official Correspondent

Ian Cadieux

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Proscia, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K243871 Philips Medical Systems Nederland B.V. Philips IntelliSite Pathology Solution 5.1 2025-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025774973. Last updated year: 2026. Please use registration number 3025774973 when referencing this establishment in official correspondence.
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