Weck Endoscopy
Country not established
- Devices
- 4
What Weck Endoscopy makes
Weck Endoscopy manufactures endoscopes and accessories, as well as endoscopic scissors with disposable or reusable shafts, and ECO ligating clips.
The company's products are Class II devices listed in the FDA 510(k) registry, and Weck Endoscopy is based in the US.
Catalogue
Endoscope And Accessories Ref K926223
Regimes: 510(k) Registry: 510(k)Endoscope And Accessories Ref K930082
Regimes: 510(k) Registry: 510(k)Endoscopic Scissors (Disposable/Reusable Shafts) Ref K926203
Regimes: 510(k) Registry: 510(k)Eco Ligating Clip Ref K930550
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Weck Endoscopy have in the registry?
The registry currently lists 4 devices for Weck Endoscopy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Weck Endoscopy's devices?
Among its 4 most recently registered devices, Weck Endoscopy has devices listed in FDA 510(k) (4 devices).
What risk classes do Weck Endoscopy's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Weck Endoscopy's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Weck Endoscopy in the registry?
The most recently registered devices listed for Weck Endoscopy include ENDOSCOPE AND ACCESSORIES, ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS) and ECO LIGATING CLIP.