Pivot Health Technologies Inc

FDA Device Registration & Listing · San Carlos, CA, US · Registration 3014023337

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
3014023337
FEI Number
3014023337
Entity Name
Pivot Health Technologies Inc
City/State/Country
San Carlos, CA, US
Establishment Address
1010 Commercial Street, Suite C, San Carlos, CA 94070, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Pivot Health Technologies Inc. (Owner Number: 10055866)
Owner / Operator Contact Address
1010 Commercial Street, Suite C, San Carlos, CA 94070, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K171408
PMA Number
N/A

All Registered Proprietary Names

Pivot Breath Sensor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2017-10-13

Official Correspondent

Daniel Balbierz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Pivot Health Technologies Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014023337. Last updated year: 2026. Please use registration number 3014023337 when referencing this establishment in official correspondence.
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