Data / Medical devices / Camera, Television, Microsurgical, Without Audio
Camera, Television, Microsurgical, Without Audio (FWD): 7 FDA-registered makers in 4 countries
7 establishments in 4 countries are registered with the FDA to make Camera, Television, Microsurgical, Without Audio (product code FWD, 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 5 510(k) clearances under this code, the latest on April 5, 1989, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- FWD
- Device class
- 1
- Regulation
- 878.4160
- Medical specialty
- General, Plastic Surgery
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Argentina | 1 |
| Germany | 1 |
| Spain | 1 |
Makers of Camera, Television, Microsurgical, 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 |
|---|---|---|---|---|---|---|---|---|
| Ecleris SRL | Villa Martelli Buenos Aires, Argentina | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eusa Global LLC | Medley, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebumedical GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marina Medical Instruments, Inc. | Davie, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| National Advanced Endoscopy Devices, Inc. | Canoga Park, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Optomic Espana, S.A. | COLMENAR VIEJO Madrid(Province), Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Perioview, LLC | Surprise, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated April 5, 1989. 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.