OMNICELL, INC.

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3015426639

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
3015426639
FEI Number
3015426639
Entity Name
OMNICELL, INC.
City/State/Country
Milpitas, CA, US
Establishment Address
725 Sycamore Drive, Milpitas, CA 95035, 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
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Anesthesia Workstation Anesthesia-Rx

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BRY Cabinet, Table And Tray, Anesthesia Anesthesiology Class 1 868.6100 2019-02-21

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
3007880912 OMNICELL, INC. Cranberry Township, PA, 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 3015426639. Last updated year: 2026. Please use registration number 3015426639 when referencing this establishment in official correspondence.
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