Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 9 companies' records, each linked to the record.
As of Nov 14, 2026, FDA's public records list Teledyne Technologies and its 9 subsidiaries with 40 510(k) clearances. The most recent is a 510(k) clearance dated Mar 9, 2004: TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND P.
| Mar 9, 2004 | TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND PK033967 · LHQ | 510(k) clearances |
| Jul 17, 2003 | MX 300 OXYGEN MONITORK024155 · CCL | 510(k) clearances |
| Jul 17, 2003 | RX300 OXYGEN ANALYZERK024228 · CCL | 510(k) clearances |
| Jun 30, 2000 | OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130K001095 · CCL | 510(k) clearances |
| Feb 3, 2000 | TED 200T7 OXYGEN MONITORK990403 · CCL | 510(k) clearances |
| Nov 9, 1999 | TED 60T OXYGEN ANALYZERK990457 · CCL | 510(k) clearances |
| Nov 13, 1997 | TED 191K963177 · CCL | 510(k) clearances |
| Mar 31, 1997 | KALGINATE IMPRESSION MATERIALK970594 · ELW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
