Data / Medical devices / United States / Zinnanti Surgical Design Group Inc
Zinnanti Surgical Design Group Inc: FDA-registered device maker in Santa Cruz, CA, United States, 4 510(k) clearances
Zinnanti Surgical Design Group Inc is registered with the FDA (registration 3009881188) in Santa Cruz, CA, United States. It lists 7 device types. The FDA files 4 510(k) clearances under its listings, the newest dated February 28, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009881188
- Address
- 3540 Soquel Ave Suite B, Santa Cruz, CA, United States, 95062
- Owner or operator
- Zinnanti Surgical Design Group Inc (10042215)
- Roles
- Specification developer
- First device listed
- November 1, 2012
- Registered through
- 2026
- Brand names listed
- Auto Sampler Endometrial Curette, J-Tip Biopsy Forceps, Rabin Finger Protector, Zinnanti Smoke Evacuation Tubing Bovie, Zinnanti Smoke Evacuation Tubing for Hyfrecator, Zinnanti Surgical Smoke and Fluid Evacuation Electrodes, Zinnanti Surgical Smoke and Fluid Evacuator Electrodes
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Specification developer | accessdata.fda.gov |
| Coagulator-Cutter, Endoscopic, Unipolar (And Accessories) | KNF | 2 | Specification developer | accessdata.fda.gov |
| Curette, Suction, Endometrial (And Accessories) | HHK | 2 | Specification developer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Specification developer | accessdata.fda.gov |
| Forceps, Biopsy, Non-Electric | FCL | 1 | Specification developer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Specification developer | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 28, 1994 | K935947 | HI-TOPS ELECTRODES 14-8000 | KNF | Substantially Equivalent | W. J. Medical Instruments, Inc. | accessdata.fda.gov |
| June 25, 1993 | K930511 | STEALTH SURGICAL IRRIGATOR ASPIRATOR | GCJ | Substantially Equivalent | W. J. Medical Instruments, Inc. | accessdata.fda.gov |
| October 3, 1989 | K892252 | BIOPSY FORCEPS | FCL | Substantially Equivalent | Zinnanti Surgical Instruments, Inc. | accessdata.fda.gov |
| October 20, 1987 | K872908 | ENDOMETRIAL SAMPLER | HHK | Substantially Equivalent | Zinnanti Surgical Instruments, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Curette, Suction, Endometrial (And Accessories)
- All makers of Tubing, Noninvasive
- All makers of Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Accessory, Surgical Apparel
Updated February 28, 1994. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.