Pilling Weck Surgical
Country not established
- Devices
- 5
What Pilling Weck Surgical makes
Pilling Weck Surgical manufactures surgical instruments and dilators for specialized medical procedures, including esophageal dilators, speaking valves for tracheostomy patients, aortic clamp tools, heart stabilizer pads, and optical forceps for precise tissue manipulation.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) database and operate from the United States.
Catalogue
Jackson Esophageal Dilator Ref K990935
Regimes: 510(k) Registry: 510(k)Shikani-French Speaking Valve Ref K982128
Regimes: 510(k) Registry: 510(k)Pilling Weck Surgical Aortic Spoon-Jaw Clamp Ref K992174
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Optical Forceps Ref K990561
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pilling Weck Surgical have in the registry?
The registry currently lists 5 devices for Pilling Weck Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pilling Weck Surgical's devices?
Among its 5 most recently registered devices, Pilling Weck Surgical has devices listed in FDA 510(k) (5 devices).
What risk classes do Pilling Weck Surgical's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pilling Weck Surgical's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pilling Weck Surgical in the registry?
The most recently registered devices listed for Pilling Weck Surgical include JACKSON ESOPHAGEAL DILATOR, SHIKANI-FRENCH SPEAKING VALVE, PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP and PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS.