Pilling Weck Group
Country not established
- Devices
- 5
What Pilling Weck Group makes
The company manufactures reusable and disposable trocars and secondary flexible sleeves for laparoscopic and minimally invasive surgical procedures, including models with insufflation ports and take-apart instrument designs.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Reusable Trocar With Sleeve (Common) Ref K964123
Regimes: 510(k) Registry: 510(k)Pilling Weck 2 Piece Take-Apart Instruments Ref K965176
Regimes: 510(k) Registry: 510(k)Reusable Trocar With Sleeve (Common) Ref K963815
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pilling Weck Group have in the registry?
The registry currently lists 5 devices for Pilling Weck Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pilling Weck Group's devices?
Among its 5 most recently registered devices, Pilling Weck Group has devices listed in FDA 510(k) (5 devices).
What risk classes do Pilling Weck Group's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pilling Weck Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pilling Weck Group in the registry?
The most recently registered devices listed for Pilling Weck Group include PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCAR, SECONDARY TROCAR AND SLEEVE WITH INSUFFLATION PORT, REUSABLE TROCAR WITH SLEEVE (COMMON) and PILLING WECK 2 PIECE TAKE-APART INSTRUMENTS.