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Zoll Medical Corporation, World Wide Headquarters

United StatesFDA applicant, unverified

Devices
21
FDA recalls
4

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Zoll Medical Corporation, World Wide Headquarters makes

Zoll Medical Corporation manufactures automated external defibrillators (AEDs) and advanced cardiac monitors, including models with CPR feedback, Bluetooth connectivity, and software updates aligned with AHA guidelines. Devices feature options like see-through CPR visualization, wireless networking, and specialized analysis tools for cardiac arrest response.

The portfolio includes Class II and Class III medical devices, all authorised via FDA 510(k) clearance. Products are listed under US regulatory requirements and distributed globally from the company’s headquarters in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue21

Newest first, rows 1-21 of 21

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  • Zoll Propaq Md Ref K112761

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll Propaq Md Ref K102468

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Zoll E Series With Cprreadycharge Ref K091265

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series Defibrillator Ref K072923

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series With Bluetooth Dial Up Networking Ref K081081

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll R Series With 2010 Aha Guidelines Software Update Ref K110361

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series With 2010 Aha Guidlines Software Update Ref K110168

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series With See-Thru Cpr Ref K070455

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll X Series Ref K112432

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll R Series Ref K120907

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series With Spco/Spmet Option Ref K092598

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series 12SL, Analysis Option Ref K080232

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll Fully Automatic Aed Plus Ref K120406

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll Propaq Md Ref K100654

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Zoll Aed Plus With 2010 Aha Guidlines Software Update Ref K110154

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series Ref K111594

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll E Series Ref K133239

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll X Series Ref K133269

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll Aedpro With See-Thru Cpr, Model Aedpro Ref K071025

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Zoll Rescuenetlink Ref K111296

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Zoll Propaq M Ref K102174

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-21 of 21

FDA recalls4

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 4 recalls initiated by Zoll Medical Corporation, World Wide Headquarters, the earliest on 2008-01-15 and the most recent on 2010-03-24. By recorded status: 4 terminated. The reasons filed fall into these groups: electrical or power. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2010

    • 24 Mar 2010 Z-1547-2010 Unclassified (pre-2012) Terminated Device issued Shock Advised message but failed to auto-charge the defibrillator. Distribution: Worldwide Distribution -- United States, Australia, Germany, Libyan Arab Jamahiriya, Malaysia, Singapore, United Arab…
      Full distribution text Worldwide Distribution -- United States, Australia, Germany, Libyan Arab Jamahiriya, Malaysia, Singapore, United Arab Emirates and the United Kingdom.
      Submission number: K042007

  • 2009

    • 31 Aug 2009 Z-2315-2009 Unclassified (pre-2012) Terminated Failure of Device to display ECG could delay delivery of defibrillation or pacing therapy. Distribution: Worldwide Distribution -- USA, UK, Austria, Australia,, Canada, Switzerland, Germany, France, French Guiana, Jordan,…
      Full distribution text Worldwide Distribution -- USA, UK, Austria, Australia,, Canada, Switzerland, Germany, France, French Guiana, Jordan, Macedonia, Netherlands, Panama, Poland, Romania, and Saudi Arabia.
      Submission number: K060559
    • 12 Feb 2009 Z-1206-2009 Unclassified (pre-2012) Terminated Device fails to discharge the defibrillation energy. Distribution: Worldwide distribution Submission number: K033474

  • 2008

    • 15 Jan 2008 Z-1167-2008 Unclassified (pre-2012) Terminated Incorrect Patient Records: Patient records that have been stored, then later transmitted or printed may not be the correct record. Records that are transmitted or printed immediately following acquisition are correct. Distribution: Worldwide Distribution including USA and countries of Canada, AE, Australia, Belgium, Chile, Germany, Spain, France, UK,…
      Full distribution text Worldwide Distribution including USA and countries of Canada, AE, Australia, Belgium, Chile, Germany, Spain, France, UK, Hungary, India, Italy, Jordan, Kuwait, Netherlands, Russia, Saudi Arabia, Singapore and ZA.
      Submission number: K042007

Frequently asked questions

How many devices does Zoll Medical Corporation, World Wide Headquarters have in the registry?

The registry currently lists 21 devices for Zoll Medical Corporation, World Wide Headquarters. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zoll Medical Corporation, World Wide Headquarters's devices?

Among its 21 most recently registered devices, Zoll Medical Corporation, World Wide Headquarters has devices listed in FDA 510(k) (21 devices).

What risk classes do Zoll Medical Corporation, World Wide Headquarters's devices fall under?

Among its 21 most recently registered devices, the classes recorded for Zoll Medical Corporation, World Wide Headquarters's devices are Class II and Class III. Each device page shows its own class and authorisation.

Are there FDA recall records for Zoll Medical Corporation, World Wide Headquarters?

FDA recall records list 4 recalls initiated by Zoll Medical Corporation, World Wide Headquarters, the most recent initiated on 24 Mar 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Zoll Medical Corporation, World Wide Headquarters in the registry?

The most recently registered devices listed for Zoll Medical Corporation, World Wide Headquarters include ZOLL PROPAQ MD, ZOLL E SERIES WITH CPRREADYCHARGE, ZOLL E SERIES DEFIBRILLATOR and ZOLL E SERIES WITH BLUETOOTH DIAL UP NETWORKING.

Generated automatically from registry data and not verified by a human reviewer.