Data / Medical devices / United States / Teledyne Analytical Instruments
Teledyne Analytical Instruments: FDA-registered device maker in City Industry, CA, United States, 1 510(k) clearance
Teledyne Analytical Instruments is registered with the FDA (registration 2026424) in City Industry, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 30, 2000. 2 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2026424
- Address
- a business unit of Teledyne Instruments, Inc. 16830 Chestnut Street, City Industry, CA, United States, 91748
- Owner or operator
- Teledyne Analytical Instruments (2026424)
- Roles
- Manufacturer
- First device listed
- October 28, 1992
- Registered through
- 2026
- Brand names listed
- Teledyne Oxygen Sensors
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Gas, Oxygen, Gaseous-Phase | CCL | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 30, 2000 | K001095 | OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130 | CCL | Substantially Equivalent | Teledyne Analytical Instruments | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| November 29, 2010 | 58322 | Not yet classified | Terminated | Micro-Fuel Cell Oxygen Sensor, Class RI5 Sensor Part Number: C41131-R15 Teledyne Instruments - Analytical Instruments Disposable oxygen sensors with limited useful life. These sensors are accessories to other oxygen diag | The recall was initiated because during a test on a batch of sensors on the company shipping dock, Teledyne Instruments discovered electrolyte loss from the sealing cylinder on a few sensors. This test was done pursuant to a complaint from one customer of label discoloration caused because of the electrolyte loss. The risk of a leak form the oxygen sensor wh | accessdata.fda.gov |
| October 27, 2003 | 27593 | Not yet classified | Terminated | Portable Oxygen Analyzer | Potential failure to display the battery low light to the end-user. | accessdata.fda.gov |
Compare with other makers
Updated August 11, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.