Spok, Inc. Plano Division

FDA Device Registration & Listing · Plano, TX, US · Registration 3011696573

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
3011696573
FEI Number
3011696573
Entity Name
Spok, Inc. Plano Division
City/State/Country
Plano, TX, US
Establishment Address
3000 Technology Dr Ste 400, Plano, TX 75074, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Spok, Inc. (Owner Number: 10037408)
Owner / Operator Contact Address
3000 Technology Drive, Ste 400, Plano, TX 75074, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K112047
PMA Number
N/A

All Registered Proprietary Names

Commtech Messenger Messenger

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MSX System, Network And Communication, Physiological Monitors Cardiovascular Class 2 870.2300 2011-11-17

Official Correspondent

Tony Johnson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Spok, 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
K973527 Data Critical Corp. CARDIO-PAGER SYSTEM 1998-03-31
K182637 Philips Medizin Systeme Boeblingen GmbH Philips IntelliVue XDS Software 2019-04-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011696573. Last updated year: 2026. Please use registration number 3011696573 when referencing this establishment in official correspondence.
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