Data / Medical devices / Camera, Television, Surgical, Without Audio
Camera, Television, Surgical, Without Audio (FWB): 17 FDA-registered makers in 6 countries
17 establishments in 6 countries are registered with the FDA to make Camera, Television, Surgical, Without Audio (product code FWB, Class 1, 21 CFR 878.4160). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 6 510(k) clearances under this code, the latest on January 7, 1994, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- FWB
- Device class
- 1
- Regulation
- 878.4160
- Medical specialty
- General, Plastic Surgery
Makers by country
| Country | Makers |
|---|---|
| United States | 7 |
| South Korea | 3 |
| China | 3 |
| India | 2 |
| Japan | 1 |
| Taiwan | 1 |
Makers of Camera, Television, Surgical, Without Audio
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 |
|---|---|---|---|---|---|---|---|---|
| Arthrex, Inc. | Naples, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arthrex California Technology, Incorporated | Santa Barbara, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arthrex, Inc. | Ave Maria, FL, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Barco, Inc | Duluth, GA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| D&T Inc. | Yuseong-gu Daejeon, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ikegami Tsushinki Co., Ltd. | Utsunomiya Tochigi, Japan | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kryptonite Solutions | Mumbai Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LG Electronics Inc. | Gumi-si Gyeongbuk, South Korea | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LG Electronics Nanjing New Technology Co., Ltd. | Nanjing Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MediCapture Asia Inc. Taiwan Branch | New Taipei City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Illumination International, Inc | Chatsworth, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nanjing Jusha Display Technology Co., Ltd | Nanjing Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Opticis Co.,ltd. | Seongnam-si Gyeonggi, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qed, Inc. | Lexington, KY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qingdao Hisense Medical Equipment Co.,Ltd. | Qingdao Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Staan Biomed Engineering Private Limited | COIMBATORE Tamil Nadu, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Endoscopy | San Jose, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated January 7, 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.