Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Shenzhen Desida Technology Co., Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 16, 2026: LED Light Therapy Mask (Models: T2, RLD10).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 16, 2026 | LED Light Therapy Mask (Models: T2, RLD10)K254079 · OHS | 510(k) clearances |
| Jun 6, 2025 | Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009)K251450 · BTA | 510(k) clearances |
| May 16, 2025 | Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)K244033 · BTA | 510(k) clearances |
| Mar 20, 2024 | Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009)K233901 · BTA | 510(k) clearances |
| Oct 21, 2022 | Hair Removal Device (Model: IPL-D26, IPL-D19)K221643 · OHT | 510(k) clearances |
| Aug 31, 2022 | IPL sapphire ice cooling hair remove deviceK221635 · OHT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
