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 Prothia USA, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 8, 1983: UNIVERSAL INSTRU. SET FOR NEUROVASCULAR.
| Jun 8, 1983 | UNIVERSAL INSTRU. SET FOR NEUROVASCULARK831071 · GZX | 510(k) clearances |
| May 3, 1983 | AMPLIGREFFEK830993 · GFD | 510(k) clearances |
| Mar 24, 1983 | ELPHA 500K823581 · GCJ | 510(k) clearances |
| Mar 7, 1983 | MYOGRAPH 2000K830058 · BXN | 510(k) clearances |
| Dec 30, 1982 | MYOTEST NERVE STIMULATORK823583 · BXN | 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
