Shenzhen Desida Technology Co., Ltd.
Shenzhen Desida Technology Co., Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 16, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K254079 | LED Light Therapy Mask (Models: T2, RLD10) | March 16, 2026 |
| K251450 | Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal | June 6, 2025 |
| K244033 | Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610) | May 16, 2025 |
| K233901 | Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009) | March 20, 2024 |
| K221643 | Hair Removal Device (Model: IPL-D26, IPL-D19) | October 21, 2022 |
| K221635 | IPL sapphire ice cooling hair remove device | August 31, 2022 |