OMNICELL, INC.

FDA Device Registration & Listing · Cranberry Township, PA, US · Registration 3007880912

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
3007880912
FEI Number
3007880912
Entity Name
OMNICELL, INC.
City/State/Country
Cranberry Township, PA, US
Establishment Address
500 Cranberry Woods Dr., Suite 400, Cranberry Township, PA 16066, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Omnicell, Inc. (Owner Number: 10059398)
Owner / Operator Contact Address
500 Cranberry Woods Drive, Cranberry Township, PA 16066, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

IVX Station IVX Cloud IVX Manager

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NEP System/Device, Pharmacy Compounding General Hospital Class 2 880.5440 2019-12-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3015426639 OMNICELL, INC. Milpitas, CA, US
3011278888 OMNICELL, INC. Warrendale, PA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007880912. Last updated year: 2026. Please use registration number 3007880912 when referencing this establishment in official correspondence.
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