Pro-Pak
Country not established
- Devices
- 3
What Pro-Pak makes
Pro-Pak manufactures sterile single-use kits for post-operative and procedural care, including suture removal, tracheostomy maintenance, and catheter care. These kits are designed for clinical use in hospital and outpatient settings to support wound management and patient recovery.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are based in the United States.
Catalogue
Sterile Suture Removal Kit Ref K821502
Regimes: 510(k) Registry: 510(k)Sterile Tracheostomy Care Kit Ref K821501
Regimes: 510(k) Registry: 510(k)Sterile Cath Care Kit Ref K821500
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro-Pak have in the registry?
The registry currently lists 3 devices for Pro-Pak. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro-Pak's devices?
Among its 3 most recently registered devices, Pro-Pak has devices listed in FDA 510(k) (3 devices).
What risk classes do Pro-Pak's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pro-Pak's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pro-Pak in the registry?
The most recently registered devices listed for Pro-Pak include STERILE SUTURE REMOVAL KIT, STERILE TRACHEOSTOMY CARE KIT and STERILE CATH CARE KIT.