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Teledyne Analytical Instruments

United Statesfrom the FDA registration address FDA establishment FEI 2026424

Devices
3
Registrations
FDA
FDA recalls
1

Catalogue3

Newest first, rows 1-3 of 3

Company details

FDA FEI number
2026424
Address
a business unit of Teledyne Instruments, Inc., City Industry, CA, 91748

FDA recalls1

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

  • 2003

    • 27 Oct 2003 Z-0145-04 Unclassified (pre-2012) Terminated Potential failure to display the battery low light to the end-user. Distribution: FL, CA, UT, AZ and MO. New Zealand, Australia, Canada and the United Kingdom

Frequently asked questions

How many devices does Teledyne Analytical Instruments have in the registry?

The registry currently lists 3 devices for Teledyne Analytical Instruments. Devices recorded under merged duplicate company entries are counted once.

Which registries list Teledyne Analytical Instruments's devices?

Among its 3 most recently registered devices, Teledyne Analytical Instruments has devices listed in FDA 510(k) (3 devices).

What risk classes do Teledyne Analytical Instruments's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Teledyne Analytical Instruments's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Teledyne Analytical Instruments?

FDA recall records list 1 recall initiated by Teledyne Analytical Instruments, the most recent initiated on 27 Oct 2003. 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 Teledyne Analytical Instruments in the registry?

The most recently registered devices listed for Teledyne Analytical Instruments include RX300 OXYGEN ANALYZER, OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2, T4, T7 & UFO130 and MX 300 OXYGEN MONITOR.

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

This is an FDA establishment record. No EUDAMED registration is known for this company.