Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011278888

FEI Number

3011278888

Entity Name

OMNICELL, INC.

City/State/Country

Warrendale, PA, US

Establishment Address

51 Pennwood Place, Warrendale, PA 15086, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Omnicell, Inc. (Owner Number: 10059398)

Owner / Operator Contact Address

500 Cranberry Woods Drive, Cranberry Township, PA 16066, US

Initial Importer Flag

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
3007880912	OMNICELL, INC.	Cranberry Township, PA, US

Similar Registrations

Registration Number	Establishment Name	Location
3006227536	ARxIUM Inc.	WINNIPEG Manitoba, CA
3006153342	Omnicell S.R.L.	TRIESTE, IT
1416980	BAXTER HEALTHCARE CORPORATION	ROUND LAKE, IL, US
2521402	B. BRAUN MEDICAL INC.	BETHLEHEM, PA, US
2523676	B. BRAUN US DEVICE MANUFACTURING LLC	ALLENTOWN, PA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011278888. Last updated year: 2026. Please use registration number 3011278888 when referencing this establishment in official correspondence.