sensiFirm
K170637 is the FDA 510(k) clearance record for sensiFirm, a class II device, cleared for El Global Trade, Ltd. on under FDA product code PBX (Massager, Vacuum, Radio Frequency Induced Heat). FDA's definition for product code PBX reads: "Generates heat in body tissues for minor relief of minor aches and pain. Mechanical massaging to provide a temporary reduction in the appearance of cellulite". FDA records list 12 510(k) clearances for El Global Trade, Ltd., from to . As of , FDA records show no recalls naming K170637.
Clearance record
- Decision date
- Received
- (134 days to decision)
- Product code
- PBX Massager, Vacuum, Radio Frequency Induced Heat
- Regulation
- 21 CFR 878.4400
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- El Global Trade, Ltd. 8 Tzoran St., P.O.Box 8242, Netanya, IL
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code PBX
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 2 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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