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 14, 2026, FDA's public records list Holl Meditronics, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 1996: ARCO-MBC, ARCO MC.
| Apr 30, 1996 | ARCO-MBC, ARCO MCK954171 · GEI | 510(k) clearances |
| Nov 9, 1994 | SONOCA IIIK942095 · LFL | 510(k) clearances |
| Jul 9, 1991 | ILCO INFRARED LIGHT COAGULATORK911600 · KNS | 510(k) clearances |
| Nov 27, 1990 | MOTO-MED RF-II AND PICOK893924 · BXB | 510(k) clearances |
| Jul 3, 1990 | SONOCA II ULTRASONIC SURGICAL DEVICEK901737 · LFL | 510(k) clearances |
| Nov 14, 1989 | SONOCA ULTRASONIC SURGICAL SYSTEMK893926 · LFL | 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
