Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of CONMEDLabelled by claude-sonnet-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 14, 2026, FDA's public records list Concept Inc. with 83 510(k) clearances. The most recent is a 510(k) clearance dated May 1, 1992: CONCEPT ENDOSTEAL FIXATION DEVICE.
| May 1, 1992 | CONCEPT ENDOSTEAL FIXATION DEVICEK912640 · HWC | 510(k) clearances |
| Oct 4, 1991 | CONCEPT MICROMILLK912957 · HRX | 510(k) clearances |
| Jun 5, 1990 | CONCEPT UNICOMPARTMENTAL KNEE SYSTEMK896648 · HSX | 510(k) clearances |
| Aug 30, 1989 | STAPLE FIXATION SYSTEMK894929 · JDR | 510(k) clearances |
| Aug 1, 1989 | INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K892376 · HRX | 510(k) clearances |
| May 8, 1989 | PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBEK891109 · KNT | 510(k) clearances |
| Nov 9, 1988 | CONCEPT POWER SYSTEMK881954 · HSZ | 510(k) clearances |
| Nov 8, 1988 | CONCEPT CCT-5200, THERMAL THERAPY SYSTEMK884255 · ILO | 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
