Data / Medical devices / China / Shenzhen Perfect Idea Technology Limited
Shenzhen Perfect Idea Technology Limited: FDA-registered device maker in Shenzhen Guangdong, China, 4 510(k) clearances
Shenzhen Perfect Idea Technology Limited is registered with the FDA (registration 3017619615) in Shenzhen Guangdong, China. It lists 10 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 18, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017619615
- Address
- 4TH Floor, Building 1, Tangwei Fuhua Industrial Park, Fuyong Bao'an, Shenzhen Guangdong, China, 518103
- Owner or operator
- Shenzhen Perfect Idea Technology Limited (10078418)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- October 21, 2020
- Registered through
- 2026
- Brand names listed
- Aglaia LED Beauty Device (BP-D2309), BP-0152,BP-012,BP-008,BP-008PLUS,BP-209,BP-1831,BP-1933,BP-215,BP-016,BP-E026,BP-206,BP-1932,BP-T02,BP-T10,BP-T13,, BP-1068, BP-1701, BP-1713, BP-A006, BP-A017, BP-A011, BP-WS05, BP-609, BP-A008,, BP-1703, BP-1803, BP-216, BP-1936, BP-1711, BP-222N, BP-222P, BP-9927, BP-9928, BP-9929, BP-9930, BP-9931, BP-9932,, BP-1705, BP-1806, BP-010, BP-010PLUS, BP-010E, BP-205, BP-1832, BP-1937, BP-1801, BP-2201, BP-S1, BP-S2, BP-S3, BP-S4, BP-S5, BP-S6, BP-S7, BP-S8,, BP-9933, BP-9934, BP-9935, BP-9936, BP-9937, BP-9938, BP-9939, BP-9940, BP-1046, BP-1048, BP-B001, BP-WS06, BP-T06,, BP-S9, BP-S10, BP-S11, BP-S12, BP-S13, BP-S14, BP-S15, BP-S16, BP-S17, BP-S18, BP-S19, BP-S20 and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 18, 2025 | K250413 | Aglaia LED Beauty Device (BP-D2309) | OHS | Substantially Equivalent | Shenzhen Perfect Idea Technology Limited | accessdata.fda.gov |
| July 22, 2022 | K220064 | Synergy Marble (Model: Opasm) | OHS | Substantially Equivalent | Yrs Group, Inc. | accessdata.fda.gov |
| June 30, 2022 | K221569 | Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K | OHT | Substantially Equivalent | Shenzhen Fansizhe Science and Technology Co., Ltd. | accessdata.fda.gov |
| June 29, 2021 | K210954 | Synergy | OHS | Substantially Equivalent | Yrs Group, Inc. | accessdata.fda.gov |
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Updated March 18, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.