Data / Medical devices / Saw, Electrically Powered
Saw, Electrically Powered (DWI): 11 FDA-registered makers in 6 countries
11 establishments in 6 countries are registered with the FDA to make Saw, Electrically Powered (product code DWI, Class 1, 21 CFR 878.4820). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on July 30, 1991, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- DWI
- Device class
- 1
- Regulation
- 878.4820
- Medical specialty
- General, Plastic Surgery
Makers by country
| Country | Makers |
|---|---|
| Germany | 5 |
| China | 2 |
| Switzerland | 1 |
| Pakistan | 1 |
| Japan | 1 |
| United States | 1 |
Makers of Saw, Electrically Powered
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 |
|---|---|---|---|---|---|---|---|---|
| Aesculap AG | TUTTLINGEN, DONAU Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bien-Air Surgery SA | Le Noirmont Jura, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Falcon Surgical Co. (Pvt.) Ltd. | Sialkot Punjab, Pakistan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guizhou Zirui Technology Co., Ltd. | Tongzi County, Zunyi Guizhou, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebumedical GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heinrich Medizintechnik GMBH | Stuttgart Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nakanishi Inc. | Kanuma Tochigi, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nopa Instruments, Medizintechnik GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Princeton Medical Group, Inc. | Franklin, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reda Instrumente GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wuhu Ruijin Medical Instrument & Device Co., Ltd. | Wuhu Anhui, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated July 30, 1991. 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.