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 Invitrocare with 10 510(k) clearances. The most recent is a 510(k) clearance dated Dec 26, 2002: ISOCARE ONE STEP SPERM PROCESSING MEDIUM CAT# 2207-12.
| Date | Record | Source |
|---|---|---|
| Dec 26, 2002 | ISOCARE ONE STEP SPERM PROCESSING MEDIUM CAT# 2207-12K023222 · MQL | 510(k) clearances |
| Jan 17, 2001 | HYALURONIDASE REAGENT, MODEL CAT#2212K003751 · MQL | 510(k) clearances |
| Aug 14, 2000 | PVP-POLYVINYLPYRROLIDONE REAGENT, MODEL CAT#2210K001967 · MQL | 510(k) clearances |
| Jun 13, 2000 | IVC THREE BLASTOCYST MEDIUM, CAT # 2007K001113 · MQL | 510(k) clearances |
| Jun 8, 2000 | SPERM WASH MEDIUM, CAT# 2003/2005K000989 · MQL | 510(k) clearances |
| May 25, 2000 | IVC TWO MEDIUMK000937 · MQL | 510(k) clearances |
| May 25, 2000 | IVC ONE MEDIUMK000938 · MQL | 510(k) clearances |
| May 25, 2000 | Q-HTF, CAT# 2001K993484 · MQL | 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
