Data / Medical devices / United States / Prosurg, Inc
Prosurg, Inc: FDA-registered device maker in San Jose, CA, United States, 4 510(k) clearances
Prosurg, Inc is registered with the FDA (registration 3006789154) in San Jose, CA, United States. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 11, 2016. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3006789154
- Address
- 2193 Trade Zone Blvd, San Jose, CA, United States, 95131
- Owner or operator
- Neoscope2020 LLC / dba Prosurg inc (10022651)
- Roles
- Manufacturer
- First device listed
- October 9, 2012
- Registered through
- 2026
- Brand names listed
- Neo-Arthroscope, NeoScope, Neoscope -3D, RF electrode family, Salinetrode, Signature series, salinetrode, salinetrode flex, NeoScope,laserTx,Signature Series, PercuTx, GelTx,Minisling, Zipperre, RF electrodes, salinetrodeflex
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Arthroscope | HRX | 2 | Manufacturer | accessdata.fda.gov |
| Cystoscope And Accessories, Flexible/Rigid | FAJ | 2 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| July 11, 2016 | K152511 | Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula | HRX | Substantially Equivalent | Prosurg, Inc. | accessdata.fda.gov |
| April 29, 2016 | K152619 | Neoscope 3D - 3D Digital Video Endoscopic System (Rigid/Flexible) | GCJ | Substantially Equivalent | Prosurg, Inc. | accessdata.fda.gov |
| September 11, 2012 | K120766 | ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION) | FAJ | Substantially Equivalent | Prosurg, Inc. | accessdata.fda.gov |
| November 12, 1996 | K962593 | ELECTROSURGICAL PROBES & DEVICES | GEI | Substantially Equivalent | Ximed/Prosure/Injectx | accessdata.fda.gov |
Compare with other makers
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Arthroscope
- All makers of Cystoscope And Accessories, Flexible/Rigid
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
Updated July 11, 2016. 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.