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 Chalgren Enterprises with 21 510(k) clearances. The most recent is a 510(k) clearance dated Jun 22, 1999: FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550.
| Date | Record | Source |
|---|---|---|
| Jun 22, 1999 | FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550K982950 · IKT | 510(k) clearances |
| Jun 13, 1996 | RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STPK960591 · IKT | 510(k) clearances |
| Jan 29, 1996 | DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODEK955335 · IKT | 510(k) clearances |
| Jan 22, 1996 | EMG DISC RECORDING ELECTRODEK953354 · GXY | 510(k) clearances |
| Jan 22, 1996 | EMG RECORDING RING ELECTRODEK953356 · GXY | 510(k) clearances |
| Jan 22, 1996 | EMG DISC RECORDING ELECTRODEK953361 · GXY | 510(k) clearances |
| Dec 6, 1995 | EMG DISC RECORDING ELECTRODE WITH PINK952908 · GXY | 510(k) clearances |
| Dec 6, 1995 | EMG DISC RECORDING ELECTRODE WITH PINK952690 · GXY | 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
