# International Life Sciences

- Location (FDA's records): Marietta, GA
- FDA decisions: 4 (2019–2026): 4 510(k) clearances
- Product codes: MBI (1), FTL (1), OWW (1), QWJ (1)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 7 (3 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Parcus Medical, LLC: 1 (https://510kreport.com/company/parcus-medical)
- Smith & Nephew Endoscopy, Inc.: 1 (https://510kreport.com/company/smith-nephew-endoscopy)
- Artimplant AB: 1 (https://510kreport.com/company/artimplant)
- Fibralign Corporation: 1 (https://510kreport.com/company/fibralign)

## Firms that cite its devices most
- Xiros, Ltd.: 2 (https://510kreport.com/company/xiros)
- Conmed Corporation: 1 (https://510kreport.com/company/conmed)
- Theramicro: 1 (https://510kreport.com/company/theramicro)

## Its most-cited devices
- K192112: FlexBand Plus (2019), cited by 3
- K200503: ATL Anchors (2020), cited by 2
- K230316: FlexBand; FlexPatch; FlexBand Plus (2023), cited by 2

## Recent decisions
- K260317: Artelon Convenience Kits (Apr 9, 2026)
- K230316: FlexBand; FlexPatch; FlexBand Plus (May 26, 2023)
- K200503: ATL Anchors (Sep 2, 2020)
- K192112: FlexBand Plus (Sep 27, 2019)

Source page: https://510kreport.com/company/international-life-sciences