Pilling Weck, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Pilling Weck, Inc. makes
Pilling Weck, Inc. makes surgical instruments and devices including congenital thoracoscopy instruments, multipolar scissors and cables, surgical staplers, Y stent forceps, hemostatic clip systems, and disposable automatic hemoclips.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Burke Congenital Thoracoscopy Instruments Ref K962771
Regimes: 510(k) Registry: 510(k)Versastat Multipolar Scissors And Cables Ref K974250
Regimes: 510(k) Registry: 510(k)Visistat Stapler Ref K943719
Regimes: 510(k) Registry: 510(k)Pilling Weck Surgical Y Stent Forceps Ref K990547
Regimes: 510(k) Registry: 510(k)Hemoclip Ecosystem Ref K945520
Regimes: 510(k) Registry: 510(k)Pilling Weck M-20 Disposable Automatic Hemoclip Ref K944552
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pilling Weck, Inc. have in the registry?
The registry currently lists 6 devices for Pilling Weck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pilling Weck, Inc.'s devices?
Among its 6 most recently registered devices, Pilling Weck, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Pilling Weck, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Pilling Weck, Inc.'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, Inc. in the registry?
The most recently registered devices listed for Pilling Weck, Inc. include BURKE CONGENITAL THORACOSCOPY INSTRUMENTS, VERSASTAT MULTIPOLAR SCISSORS AND CABLES, VISISTAT STAPLER and PILLING WECK SURGICAL Y STENT FORCEPS.