| Primary Device ID | 06933917000853 |
| NIH Device Record Key | bc1c1275-2e8d-4414-bdfc-7a248d9fc266 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fittop |
| Version Model Number | FCM902 |
| Company DUNS | 544301417 |
| Company Name | Shenzhen Fittop Health Technology Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06933917000853 [Primary] |
| OHS | Light Based Over The Counter Wrinkle Reduction |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-10-03 |
| Device Publish Date | 2025-09-25 |
| 06933917000884 | FCM908 |
| 06933917000877 | FCM906 |
| 06933917000860 | FCM905 |
| 06933917000853 | FCM902 |
| 06933917000846 | FCM910 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FITTOP 97450694 not registered Live/Pending |
SHENZHEN FITTOP HEALTH TECHNOLOGY CO.,LTD. 2022-06-09 |
![]() FITTOP 97450657 not registered Live/Pending |
SHENZHEN FITTOP HEALTH TECHNOLOGY CO.,LTD. 2022-06-09 |
![]() FITTOP 90270553 not registered Live/Pending |
Zhao Xiahuai 2020-10-22 |
![]() FITTOP 88934092 not registered Live/Pending |
SHENZHEN FITTOP HEALTH TECHNOLOGY CO.,LTD. 2020-05-26 |
![]() FITTOP 86666330 4889423 Live/Registered |
SHENZHEN FITTOP HEALTH TECHNOLOGY CO., LTD. 2015-06-18 |