Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled 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 15, 2026, FDA's public records list Swemed Lab International AB with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 30, 2006: CLEAR VISION EMBRYO TRANSFER CATHETER SET, MODEL B100000 - B 100007; CLEAR VISION TRIAL ….
| Jan 30, 2006 | CLEAR VISION EMBRYO TRANSFER CATHETER SET, MODEL B100000 - B 100007; CLEAR VISION TRIAL TRANSFER CATHETER SETK053208 · MQF | 510(k) clearances |
| Nov 5, 2002 | BLASTOMERE BIOPSY PIPETTE, MODELS H-55530 AND H-55540K022643 · MQH | 510(k) clearances |
| Aug 18, 1999 | SWEMED FOLLICLE ASPIRATION SET, DOUBLE LUMEN, SINGLE LUMEN, AND LUER NEEDLEK991273 · MQE | 510(k) clearances |
| Jul 19, 1999 | SWEMED INTRACYTOPLASMIC SPERM INJECTION (ICSI) MICRO-INJECTION PIPETTES; HOLDING PIPTTES; DENUDING PIPETTES; ASSISTED/ZOK991700 · MQH | 510(k) clearances |
| Oct 3, 1994 | SWEMED NEEDLE GUIDEK925999 · IYO | 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
