# Swemed Lab International AB

- Location (FDA's records): Billdal, SE
- FDA decisions: 4 (1999–2006): 4 510(k) clearances
- Product codes: MQH (2), MQF (1), MQE (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- CooperSurgical, Inc.: 3 (https://510kreport.com/company/coopersurgical)
- Cooper Surgical: 3 (https://510kreport.com/company/cooper-surgical)

## Firms that cite its devices most
- Vitrolife Sweden AB: 2 (https://510kreport.com/company/vitrolife-sweden)
- Brinkmann Instruments, Inc.: 1 (https://510kreport.com/company/brinkmann-instruments)
- Kitazato Medical Co., Ltd.: 1 (https://510kreport.com/company/kitazato-medical)

## Its most-cited devices
- K991273: Swemed Follicle Aspiration Set, Double Lumen, Single Lumen, and Luer Needle (1999), cited by 3
- K991700: Swemed Intracytoplasmic Sperm Injection (Icsi) Micro-Injection Pipettes; Holding Pipttes; Denuding Pipettes; Assisted/ZO (1999), cited by 1

## Recent decisions
- K053208: Clear Vision Embryo Transfer Catheter Set, Model B100000 - B 100007; Clear Vision Trial Transfer Catheter Set (Jan 30, 2006)
- K022643: Blastomere Biopsy Pipette, Models H-55530 and H-55540 (Nov 5, 2002)
- K991273: Swemed Follicle Aspiration Set, Double Lumen, Single Lumen, and Luer Needle (Aug 18, 1999)
- K991700: Swemed Intracytoplasmic Sperm Injection (Icsi) Micro-Injection Pipettes; Holding Pipttes; Denuding Pipettes; Assisted/ZO (Jul 19, 1999)

Source page: https://510kreport.com/company/swemed-lab-international