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 13, 2026, FDA's public records list Conception Technologies with 8 510(k) clearances. The most recent is a 510(k) clearance dated Apr 8, 2003: ENHANCE HUMAN SERUM ALBUMIN.
| Date | Record | Source |
|---|---|---|
| Apr 8, 2003 | ENHANCE HUMAN SERUM ALBUMINK030850 · MQL | 510(k) clearances |
| Dec 13, 2002 | ENHANCE HTF MEDIUM WITH HEPESK023655 · MQL | 510(k) clearances |
| Dec 13, 2002 | SPERM WASH MEDIUM WITH GENTAMICINK023717 · MQL | 510(k) clearances |
| Mar 28, 2002 | PBS, PBSW WITH CATIONS AND PHENOL REDK020490 · MQL | 510(k) clearances |
| Jul 2, 2001 | HYALURONIDASE IN HTF MEDIUM; HYALURONIDASE IN EBSS MEDIUMK011573 · MQL | 510(k) clearances |
| Jul 2, 2001 | 10% PVP; 10% PVP IN EBSS SOLUTIONK011481 · MQL | 510(k) clearances |
| Jun 13, 2001 | OIL FOR TISSUE CULTUREK011462 · MQL | 510(k) clearances |
| Aug 2, 2000 | WATER FOR TISSUE CULTURE, MODELS 1500K993140 · MTW | 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
