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 E & M Engineering, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 10, 1999: DISPOSABLE ELECTROSURGERY GROUNDING PAD.
| Feb 10, 1999 | DISPOSABLE ELECTROSURGERY GROUNDING PADK984276 · GEI | 510(k) clearances |
| Jul 31, 1996 | LOOP/SQUARE ELECTRODEK952030 · HGI | 510(k) clearances |
| Feb 10, 1995 | BLADE ELECTRODEK945531 · GEI | 510(k) clearances |
| Jun 13, 1994 | ELECTROSURGICAL PENCILK936304 · GEI | 510(k) clearances |
| Jun 6, 1994 | REUSABLE, HAND CONTROLLED ESPK936075 · GEI | 510(k) clearances |
| Jul 2, 1993 | ELECTROSURGICAL UNITK921271 · GEI | 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
