HP Inc

FDA Device Registration & Listing · Fort Collins, CO, US · Registration 1000263389

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
1000263389
FEI Number
1000263389
Entity Name
HP Inc
City/State/Country
Fort Collins, CO, US
Establishment Address
3390 E HARMONY RD, Fort Collins, CO 80528, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
HP Inc. (Owner Number: 10041591)
Owner / Operator Contact Address
3390 East Harmony Road, Fort Collins, CO 80528, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Z2 Mini G1i (B7SV4AV) Z2 Tower G1i (B7SV6AV) Z2 Mini G1a (B7SV3AV) HP Z8 Fury G6i Workstation (D20WRAV) Z230 (E9H74AV) Z440 (G8W00AV) Z640 (G8W05AV) Z1 G2 (J5V15AV) Z840 (G8W10AV) Z240 (M6V41AV) Z1 G3 (T0J59AV) Z2 Mini (X8V11AV) Z8 G4 (1AK64AV) Z4 G4 (1JQ69AV) Z6 G4 (1AM16AV) Z2 Mini G4 (3AX82AV) Z2 SFF G4 (2ZP77AV) Z2 Tower G4 (2ZR32AV) Z2 Tower G5 (9FV44AV) ZCentral 4R (9DX50AV) Z2 SFF G5 (9FX25AV) Z2 G8 SFF (275B6AV) Z2 Mini G5 (9JE23AV) Z2 G8 Tower (28A88AV) Z1 (D4H09AV) Z220 (D4H10AV) Z8 Fury G5 (7J9Z8AV) Z820 (D4H13AV) Z6 G5 (7J9Z1AV) Z6 G5 A (7K002AV) Z2 Tower G9 (6Z428AV) Z2 Mini G9 (4Z6E2AV) Z620 (D4H12AV) Z2 SFF G9 (6Z422AV) Z420 (D4H11AV) Z8 G5 (7J9Z4AV) Z4 G5 (7J9Y8AV) Z4 Rack G5 (7J9Y5AV) HP Z4 G6i Workstation (D20X1AV) Z2 SFF G1i (B7SV5AV)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMB Device, Digital Image Storage, Radiological Radiology Class 1 892.2010 2012-08-09

Official Correspondent

Rick Duran

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000263389. Last updated year: 2026. Please use registration number 1000263389 when referencing this establishment in official correspondence.
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