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 Eder Instrument Co., Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Dec 14, 1984: BIPOLAR SUCTION ELECTRODE.
| Dec 14, 1984 | BIPOLAR SUCTION ELECTRODEK843498 · GET | 510(k) clearances |
| Oct 31, 1984 | ARTHROSCOPY LEG HOLDERK843499 · | 510(k) clearances |
| Oct 31, 1984 | SURGICAL KNIVES & PROBESK843497 · EMF | 510(k) clearances |
| Sep 12, 1983 | LARYNGOSCOPE ATTACHMENT PH2000K831255 · EQN | 510(k) clearances |
| Jul 26, 1983 | LASER BRONCHOSCOPEK831240 · EOQ | 510(k) clearances |
| Jun 10, 1983 | LASER LAPARAXOPEK831241 · HET | 510(k) clearances |
| Oct 22, 1982 | ENDOSCOPIC VIDEOSYSTEMK822959 · FET | 510(k) clearances |
| Oct 31, 1980 | SURGICAL KNIVES & PROBESK802479 · HXB | 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
