J. Sklar Mfg. Co., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 18
What J. Sklar Mfg. Co., Inc. makes
J. Sklar Mfg. Co., Inc. manufactures surgical and diagnostic instruments including endoscopes, forceps, clamps, ligators, scissors, and suction units for use in procedures such as hemorrhoid treatment, fallopian tube stabilization, hysterectomy, fetal heart monitoring, and biopsy.
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
Search and filter all 18 devicesFrequently asked questions
How many devices does J. Sklar Mfg. Co., Inc. have in the registry?
The registry currently lists 18 devices for J. Sklar Mfg. Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list J. Sklar Mfg. Co., Inc.'s devices?
Among its 18 most recently registered devices, J. Sklar Mfg. Co., Inc. has devices listed in FDA 510(k) (18 devices).
What risk classes do J. Sklar Mfg. Co., Inc.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for J. Sklar Mfg. Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from J. Sklar Mfg. Co., Inc. in the registry?
The most recently registered devices listed for J. Sklar Mfg. Co., Inc. include KOGAN ENDOSPECULUM 9-1/2, RUDD-CLINIC HEMORRHOIDAL FORCEPS, MINICLAMPS, STABILIZ., FALLOPIAN TUBE and GUSBERG HYSTERECTOMY CLAMP.