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Zhejiang Luyao Electronics Technology Co., Ltd.
FDA Regulatory Profile
Zhejiang Luyao Electronics Technology Co., Ltd. appears in FDA public data with 1 recall, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2463-2025, Class II) was initiated on January 17, 2025. Its most recent 510(k) clearance was granted on December 22, 2022.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
| Z-2463-2025 | Class II | Brand Name: HOMEDICS Product Name: Air Compression Leg Massager Model/Catalog Number: SR-160HJ Pr | January 17, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
| K222949 | Air Compression Leg Massager (Model: LY-670D) | December 22, 2022 |