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 15, 2026, FDA's public records list Germaine Laboratories with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 26, 2005: AIMSTICK URINE REAGENT STRIPS.
| Oct 26, 2005 | AIMSTICK URINE REAGENT STRIPSK051727 · CEN | 510(k) clearances |
| Jan 22, 2002 | AIMSTEP PREGNANCYK013857 · DHA | 510(k) clearances |
| May 10, 1999 | ACCUDIP HOME PREGNANCY AND/OR AIMSTICK PREGNANCYK991369 · LCX | 510(k) clearances |
| Apr 16, 1998 | AIMSTEP COMBO PREGNANCY, 1 TEST, 30 TEST, 50 TEST, 100 TESTK981165 · JHI | 510(k) clearances |
| Mar 6, 1998 | AIMSTEP PREGNANCYK980531 · JHI | 510(k) clearances |
| Jan 2, 1998 | AIMSTICK PBD PREGNANCYK974368 · DHA | 510(k) clearances |
| Jan 2, 1998 | AIMSTICK PBD COMBO PREGNANCYK974512 · DHA | 510(k) clearances |
| Dec 19, 1997 | MIDSTREAM HOME REGNANCY TESTK973825 · DHA | 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
