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 Surgi-Quip Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 9, 1984: CHARLES/MCINTYRE GIANT BREAK TABLE.
| May 9, 1984 | CHARLES/MCINTYRE GIANT BREAK TABLEK841115 · FQO | 510(k) clearances |
| May 9, 1984 | MOBILE OPHTHALMIC OPERATING TABLEK841116 · FWX | 510(k) clearances |
| Mar 22, 1984 | WEE BAG O'MERCURYK840004 · LCC | 510(k) clearances |
| Oct 4, 1983 | ELECTRONIC UNITK832887 · EPT | 510(k) clearances |
| Sep 14, 1982 | SELF-CONTAINED MOBILE OPHTHAL. OPER. .K822427 · FSE | 510(k) clearances |
| Sep 14, 1982 | CEMENT EXTRACTION INSTRUMENTATIONK822554 · | 510(k) clearances |
| Sep 2, 1982 | SURGI-QUIP MICROSCOPE STANDK822428 · HBN | 510(k) clearances |
| Sep 2, 1982 | MCINTYRE MICROSCOPE STANDK822426 · HBN | 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
