Data / Medical devices / Fluid Jet Removal System
Fluid Jet Removal System (PZP): 5 FDA-registered makers in 2 countries
5 establishments in 2 countries are registered with the FDA to make Fluid Jet Removal System (product code PZP, Class 2, 21 CFR 876.4350). 1 of them has a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on July 9, 2026, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- PZP
- Device class
- 2
- Regulation
- 876.4350
- Medical specialty
- General, Plastic Surgery
Makers by country
| Country | Makers |
|---|---|
| United States | 3 |
| China | 2 |
Makers of Fluid Jet Removal System
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| PROCEPT BioRobotics Corporation | San Jose, CA, United States | Manufacturer, Manufacturer for export, Specification developer | 9 | July 9, 2026 | 0 | 2 | 0 | api.fda.gov |
| Myriad Fiber Imaging Technologies, Inc. | Dudley, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precision Optics Corp. | Gardner, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shantou Institute Of Ultrasonic Instruments Co., Ltd. | Shantou Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shantou Institute Of Ultrasonic Instruments Co., Ltd. | SHANTOU Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated July 9, 2026. 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.