Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 13, 2026, FDA's public records list Synermed with 45 510(k) clearances. The most recent is a 510(k) clearance dated Sep 25, 1997: SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KIT.
| Date | Record | Source |
|---|---|---|
| Sep 25, 1997 | SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KITK973109 · CIG | 510(k) clearances |
| Aug 7, 1997 | SYNERMED TOTAL BILIRUBIN REAGENT KITK972716 · CIG | 510(k) clearances |
| Jun 26, 1997 | SYNERMED IR 200 CHEMISTRY ANALYZERK971491 · JJF | 510(k) clearances |
| Mar 3, 1997 | SYNERMED ISE REAGENTSK962479 · CGZ | 510(k) clearances |
| Dec 18, 1996 | SYNERMED DIRECT BILIRUBIN REAGENT KITK963939 · CIG | 510(k) clearances |
| Mar 11, 1996 | SYNERMED ENZYMATIC CO2 REAGENT KITK960793 · KHS | 510(k) clearances |
| Aug 31, 1995 | SYNERMED CALCIUM REAGENT KITK953395 · CJY | 510(k) clearances |
| Jun 20, 1995 | SYNERMED ISE REAGENTSK952179 · JGS | 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
