Revert srl
IT-MF-000029504 · Italy · Belluno
Revert srl is registered in the European database on medical devices as a manufacturer, with 430 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 430 |
|---|
Most frequent device types declared: ACETATE FAMILY, COMBINATION FRAMES, METAL FRAMES, PLASTIC FRAMES.
Devices declared under this manufacturer
- Polar Eyewear mod Gold 1031 col. 27
- Polar Eyewear mod. 6012 col. 76
- Polar Eyewear mod. 635 Clip-on col. 428
- Polar Eyewear mod. 775 col. 08
- Polar Eyewear mod. 8007 Clip-on col. 77/Q
- Polar Eyewear mod. Enea Clip-on col. 76/G
- Polar Eyewear mod. Gold Prometeo col. 428
- Polar Eyewear model 448 col. 20 CLIP-ON
- Polar Eyewear model 535 col. 78 CLIP-ON
- Polar Eyewear model 601 col. 27 CLIP-ON
- Polar Eyewear model 602 col. 76 CLIP-N
- Polar Eyewear model GOLD C 54 CLIP-ON col. 77
Showing 12 of 430 declared devices.
Catalogue references include K53578, K60127, K601276, K77508, KCENE76/G, KG103127.
European nomenclature codes declared: Q02100202, Q02100201, Q02100203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 430 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 430 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Revert srl was not found in either the U.S. or the Canadian register.