Celfirm
510(k) K172023
Celfirm is a medical device (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by VIOL Co., Ltd., cleared under FDA 510(k) K172023 on 13 Oct 2017, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK172023 | Date13 Oct 2017 | StatusActive |
Official records
- FDA 510(k) database K172023
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GEI
- Device class
- Class II
- Regulation
- 21 CFR Part 878.4400
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K172023
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| CELFIRM | CELFIRM | 08809502330026 | On the market | |
| CONSUMABLE TIP | Consumable Tip | 28809502330013 | On the market | |
| CONSUMABLE TIP | Consumable Tip | 38809502330010 | On the market | |
| FOOT SWITCH F/S | F/S | 08809502330033 | On the market | |
| HAND PIECE H/S_02 | H/S_02 | 08809502330040 | On the market |
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