Dongguan Letme Medical Technology Co., Ltd. (manufacturer, Dongguan Guangdong, CN): 3 new FDA device listings, incl. light based over-the-counter hair removal
Dongguan Letme Medical Technology Co., Ltd. (Dongguan Guangdong): 3 new FDA device listings, incl. light based over-the-counter hair removal. Its amount of 3 is above the median of 1 (77th percentile). Dated 146 days ago, it serves as a historical benchmark. Score 75/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 3 · 77th percentile of 2,570 DeviceEstablishmentPulse records · 3.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Dongguan Letme Medical Technology Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Dongguan Guangdong, CN |
| New listings | 3 |
| Devices | Light Based Over-The-Counter Hair Removal |
| Product codes | OHT |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | 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-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W; IPL Home Use Hair Removal Device/D-1198, D-1185, D-1186, D-1189, D-1197 |
| First new listing | 2026-06-11 |
| Latest new listing | 2026-06-11 |
| FDA registration number | 3048248141 |
| Registration expires | 2026-12-31 |
| amount percentile | 77th of 2,570 (median 1, 3.0x median) |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-06-11
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Dongguan Letme Medical Technology Co., Ltd. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Dongguan Letme Medical Technology Co., Ltd.'s amount: 77th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
75 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Dongguan Letme Medical Technology Co., Ltd. in Dongguan Guangdong?
Dongguan Letme Medical Technology Co., Ltd. (Dongguan Guangdong, CN), a manufacturer, added 3 FDA device listings on 2026-06-11.
How does Dongguan Letme Medical Technology Co., Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 3 sits in the upper half (77th percentile) of 2,570 records; the median is 1. It is 146 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.
Dongguan Letme Medical Technology Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Dongguan Letme Medical Technology Co., Ltd. | Dongguan Guangdong, CN | 3 | 77th | 2026-06-11 |
| Beacon Biosignals, Inc. | Boston, MA | 3 | 77th | 2026-10-16 |
| Endovascular Engineering, Inc. | Menlo Park, CA | 3 | 77th | 2026-10-14 |
| INNO Holdings Inc. | Millcreek, UT | 3 | 77th | 2026-10-05 |
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.