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Data / Medical devices / China / Dongguan Letme Medical Technology Co., Ltd.

Dongguan Letme Medical Technology Co., Ltd.: FDA-registered device maker in Dongguan Guangdong, China, 3 510(k) clearances

Dongguan Letme Medical Technology Co., Ltd. is registered with the FDA (registration 3048248141) in Dongguan Guangdong, China. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated June 18, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3048248141
Address
Rm.502, Bldg.3,Tianan Shenchuang Valley,No.178,Fenggang Section,Dongshen Road,Fenggang Town, Dongguan Guangdong, China, 523690
Owner or operator
Dongguan Letme Medical Technology Co., Ltd. (10096044)
Roles
Manufacturer
First device listed
June 11, 2026
Registered through
2026
Brand names listed
IPL Home Use Hair Removal Device/D-1128, D-1129, D-1130, D-1119, D-1103, D-1176, D-1151, D-T1002, IPL Home Use Hair Removal Device/D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W, IPL Home Use Hair Removal Device/D-1198, D-1185, D-1186, D-1189, D-1197, IPL Home Use Hair Removal Device/D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W

Devices it lists

DeviceProduct codeClassRoleSource
Light Based Over-The-Counter Hair RemovalOHT2Manufactureraccessdata.fda.gov

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 18, 2024K240583IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)OHTSubstantially EquivalentShenzhen Beauty Every Moment Intelligent Electric Co., Ltd.accessdata.fda.gov
May 12, 2022K221001IPL Home Use Hair Removal DeviceOHTSubstantially EquivalentShenzhen Beauty Every Moment Intelligent Electric Co., Ltd.accessdata.fda.gov
September 20, 2021K211922IPL Home Use Hair Removal DeviceOHTSubstantially EquivalentShenzhen Beauty Every Moment Intelligent Electric Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 18, 2024. 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.