Edward Weck, Inc.
United StatesFDA applicant, unverified
- Devices
- 140
What Edward Weck, Inc. makes
Edward Weck, Inc. manufactures surgical instruments and endoscopic tools, including specula, needleholders, retractors, clipping devices, forceps, clamps, and vascular scissors. Their portfolio covers general surgical applications, such as tracheotomy retractors, hemostatic clips, and titanium tying forceps, as well as specialized endoscopic accessories like needleholders and clamps. The company also produces precision instruments like a finger-tip controlled pencil for surgical marking.
The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) registry, reflecting their regulatory status. The manufacturer operates from the United States.
Catalogue
Search and filter all 140 devicesShowing 1-50 of 140
Frequently asked questions
How many devices does Edward Weck, Inc. have in the registry?
The registry currently lists 140 devices for Edward Weck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Edward Weck, Inc.'s devices?
Among its 50 most recently registered devices, Edward Weck, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Edward Weck, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Edward 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 Edward Weck, Inc. in the registry?
The most recently registered devices listed for Edward Weck, Inc. include FARRIOR OVAL SPECULUM, ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705, HOOKS #'S 7600, 7602, 7603, 7616 and NEIVS TRACHEOTOMY RETRACTOR.