Data / Medical devices / Camera, Television, Endoscopic, With Audio
Camera, Television, Endoscopic, With Audio (FWG): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Camera, Television, Endoscopic, With Audio (product code FWG, Class 1, 21 CFR 878.4160). 1 of them has 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 March 7, 1994, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- FWG
- Device class
- 1
- Regulation
- 878.4160
- Medical specialty
- General, Plastic Surgery
Makers by country
| Country | Makers |
|---|---|
| Germany | 3 |
| Italy | 2 |
| United States | 1 |
Makers of Camera, Television, Endoscopic, With 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 |
|---|---|---|---|---|---|---|---|---|
| Richard Wolf GMBH | KNITTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 1 | March 7, 1994 | 0 | 0 | 0 | api.fda.gov |
| Atmos Medizintechnik GMBH & Co. KG | LENZKIRCH Baden-Wurttemberg, Germany | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inventis SRL | Padova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mahe Medical Usa | Laramie, WY, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medcare Solutions GMBH | Emmingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| THD SPA | Correggio Reggio Emilia, Italy | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 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.