The Kendall Company
Country not established
- Devices
- 10
What The Kendall Company makes
The company manufactures central venous catheters, including neonatal/pediatric peripherally inserted central catheters (PICCs), cuffed dual-lumen catheters, and triple-lumen catheters for various patient sizes. It also produces antimicrobial sponges, electronic temperature probes, and prefilled flush syringes with sterile sodium chloride solutions. Additional offerings include urinary catheters and catheter systems designed for medical procedures.
These devices are regulated under FDA Class II and unclassified (U) categories, with most requiring 510(k) clearance. The products are listed in the FDA’s 510(k) registry, and the company is based in the United States.
Catalogue
Mahurkar Oplus Catheter, Model 13.5 Fr Ref K030209
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Kerlix Md Antimicrobial Gauze Dressing Ref K990530
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Filac Fas Temp Electronic Thermometer Ref K003313
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Excilon Amd Antimicrobial Sponge Model #7088 Ref K011941
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Kendall 14.5 Fr Maxid Cuffed Dual Lumen Catheter Ref K002901
Regimes: 510(k) Registry: 510(k)Mahurkar Triple Lumen Catheter, 12 Fr Ref K020089
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Kendall Company have in the registry?
The registry currently lists 10 devices for The Kendall Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Kendall Company's devices?
Among its 10 most recently registered devices, The Kendall Company has devices listed in FDA 510(k) (10 devices).
What risk classes do The Kendall Company's devices fall under?
Among its 10 most recently registered devices, the classes recorded for The Kendall Company's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Kendall Company in the registry?
The most recently registered devices listed for The Kendall Company include MAHURKAR OPLUS CATHETER, MODEL 13.5 FR, KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325, KERLIX MD ANTIMICROBIAL GAUZE DRESSING and KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311.