# Covidien Lp, Formerly Registered AS Kendall

- Location (FDA's records): Mansfield, MA
- FDA decisions: 3 (2009–2013): 3 510(k) clearances
- Product codes: KNT (1), MSD (1), FOS (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 6 (0 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
- Biosearch Medical Products, Inc.: 1 (https://510kreport.com/company/biosearch-medical-products)
- Corpak Medsystems: 1 (https://510kreport.com/company/corpak-medsystems)
- Kendall: 1 (https://510kreport.com/company/kendall)
- Arrow International, Inc.: 1 (https://510kreport.com/company/arrow-international)
- Sherwood Medical Co.: 1 (https://510kreport.com/company/sherwood-medical)

## Firms that cite its devices most
- Covidien: 3 (https://510kreport.com/company/covidien)
- Vesco Medical, LLC: 1 (https://510kreport.com/company/vesco-medical)
- Haolang Medical USA Corporation: 1 (https://510kreport.com/company/haolang-medical-usa)
- Degania Silicone, Ltd.: 1 (https://510kreport.com/company/degania-silicone)

## Its most-cited devices
- K112511: Dobbhoff Dual Port Feeding Tube (2012), cited by 3
- K092205: Palindrome P Hemodialysis Catheter (2009), cited by 2
- K130725: Modified Argyle Polyurethane Umbilical Vessel Catheter 2.5FR, 3.5FR, 5 FR. (2013), cited by 1

## Recent decisions
- K130725: Modified Argyle Polyurethane Umbilical Vessel Catheter 2.5FR, 3.5FR, 5 FR. (Apr 17, 2013)
- K112511: Dobbhoff Dual Port Feeding Tube (May 11, 2012)
- K092205: Palindrome P Hemodialysis Catheter (Oct 30, 2009)

Source page: https://510kreport.com/company/covidien-lp-formerly-registered-as-kendall