Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Elmed Incorporated with 27 510(k) clearances. The most recent is a 510(k) clearance dated Mar 22, 2019: ELMED Laparoscopic Instruments and Accessories.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Mar 22, 2019 | ELMED Laparoscopic Instruments and AccessoriesK181173 · GCJ | 510(k) clearances |
| May 14, 2001 | DENSTATK010465 · GEI | 510(k) clearances |
| Mar 19, 1998 | ELMED ESU 120 M/M DIGITALK974793 · GEI | 510(k) clearances |
| Jan 18, 1996 | ELMED RF-ALERTK953271 · GEI | 510(k) clearances |
| Aug 14, 1995 | ELMED THERMO-FLUXK952110 · GEI | 510(k) clearances |
| Nov 15, 1994 | ELMED LBC 50-PK926517 · HIN | 510(k) clearances |
| May 2, 1994 | ELMED ESU 300 M/M AND DIGITALK932938 · GEI | 510(k) clearances |
| May 17, 1993 | ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/MK921770 · 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
