Zinnanti Surgical Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 76
What Zinnanti Surgical Instruments, Inc. makes
Zinnanti Surgical Instruments, Inc. manufactures a range of reusable surgical instruments, including thoracotomy and micro-surgery scissors, rectal and vaginal retractors, cervical dilators, biopsy forceps, ovum forceps, and dental tools like root elevators and micro cautery needles. The portfolio also includes specialized instruments like the Zeppelin scissors and Roto Fit biopsy forceps, designed for precision in surgical procedures.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. These instruments are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Search and filter all 76 devicesShowing 1-50 of 76
Frequently asked questions
How many devices does Zinnanti Surgical Instruments, Inc. have in the registry?
The registry currently lists 76 devices for Zinnanti Surgical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zinnanti Surgical Instruments, Inc.'s devices?
Among its 50 most recently registered devices, Zinnanti Surgical Instruments, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Zinnanti Surgical Instruments, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Zinnanti Surgical Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zinnanti Surgical Instruments, Inc. in the registry?
The most recently registered devices listed for Zinnanti Surgical Instruments, Inc. include SCISSORS: THOREK, JORGENSEN, FINOCHIETTO, ZEPPELIN SCISSORS, RECTAL SPECULA - CHELSEA-EATON, KELLY, MATHIEU and ZSI BIOPSY FORCEPS.