Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Clinical Technology Corp. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 1994: TEK-LUBE.
| Date | Record | Source |
|---|---|---|
| Jan 31, 1994 | TEK-LUBEK925080 · EFB | 510(k) clearances |
| Jul 6, 1988 | BIOSIGNK872867 · FRC | 510(k) clearances |
| Feb 18, 1988 | BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000K880166 · LFL | 510(k) clearances |
| Sep 1, 1987 | BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)K872705 · GEI | 510(k) clearances |
| Nov 10, 1986 | BOVIE ULTRASONIC SURGICAL SYSTEMK855138 · LBK | 510(k) clearances |
| May 2, 1986 | ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCESK854231 · GEI | 510(k) clearances |
| Sep 5, 1985 | STERI-GRIPK853507 · | 510(k) clearances |
| Aug 19, 1985 | GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBINK852986 · LCP | 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
