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 15, 2026, FDA's public records list John F. Greer Co., Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 17, 1987: E-Z LOOP.
| Apr 17, 1987 | E-Z LOOPK870577 · EXB | 510(k) clearances |
| Apr 10, 1987 | EZ TAC FILTERK870531 · EXB | 510(k) clearances |
| Jan 14, 1987 | E-Z HOLD - #4060K864190 · KMK | 510(k) clearances |
| Dec 4, 1986 | ULTRA-GEL - #4083K864189 · EXB | 510(k) clearances |
| Dec 4, 1986 | E-Z HOLD WITH ADHESIVE BASE.-#4065K864188 · KNX | 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
