Teledyne Analytical Instruments

FDA Device Registration & Listing · City Industry, CA, US · Registration 2026424

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
2026424
FEI Number
2026424
Entity Name
Teledyne Analytical Instruments
City/State/Country
City Industry, CA, US
Establishment Address
a business unit of Teledyne Instruments, Inc., 16830 Chestnut Street, City Industry, CA 91748, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Teledyne Analytical Instruments (Owner Number: 2026424)
Owner / Operator Contact Address
16830 Chestnut Street, City of Industry, CA 91748, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Teledyne Oxygen Sensors

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCL Analyzer, Gas, Oxygen, Gaseous-Phase Anesthesiology Class 2 868.1720 1992-10-28

Official Correspondent

Nino Lugue

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Teledyne Analytical Instruments
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
K072469 Digiflo, Inc. DIGIFLO CONCENTRATOR ANALYZER 2008-01-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2026424. Last updated year: 2026. Please use registration number 2026424 when referencing this establishment in official correspondence.
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