Shenzhen Langzhiyin Electronic Co.,Ltd. (manufacturer, Shenzhen Guangdong, CN): 5 new FDA device listings, incl. massager, therapeutic, manual
Shenzhen Langzhiyin Electronic Co.,Ltd. (Shenzhen Guangdong): 5 new FDA device listings, incl. massager, therapeutic, manual. Its amount of 5 is above the median of 1 (87th percentile). Dated 156 days ago, it serves as a historical benchmark. Score 60/100. 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: 5 · 87th percentile of 2,570 DeviceEstablishmentPulse records · 5.0x 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 | Shenzhen Langzhiyin Electronic Co.,Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Shenzhen Guangdong, CN |
| New listings | 5 |
| Devices | Massager, Therapeutic, Manual; Lens, Spectacle (Prescription), For Reading Discomfort; Frame, Spectacle; Sunglasses (Non-Prescription Including Photosensitive); Lens, Spectacle, Non-Custom (Prescription) |
| Product codes | LYG, NJH, HQZ, HQY, HQG |
| Device classes | Class I |
| Medical specialties | Physical Medicine, Ophthalmic |
| Brand names | MASSAGER, THERAPEUTIC, MANUAL(massage device); Lens, Spectacel(Prescription), for reading discomfort; Frame, Spectacle; OHO sunshine smart glasses (Non-prescription Including Photosensitive); Lens, Spectacle, Non-Custom(Prescription) |
| First new listing | 2026-06-02 |
| Latest new listing | 2026-06-02 |
| FDA registration number | 3018153150 |
| Registration expires | 2026-12-31 |
| amount percentile | 87th of 2,570 (median 1, 5.0x median) |
| Peer records CSV (500 CN records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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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: 2026-06-02
- 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: Shenzhen Langzhiyin Electronic Co.,Ltd. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Shenzhen Langzhiyin Electronic Co.,Ltd.'s amount: 87th 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)
60 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Shenzhen Langzhiyin Electronic Co.,Ltd. in Shenzhen Guangdong?
Shenzhen Langzhiyin Electronic Co.,Ltd. (Shenzhen Guangdong, CN), a manufacturer, added 5 FDA device listings on 2026-06-02.
How does Shenzhen Langzhiyin Electronic Co.,Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (87th percentile) of 2,570 records; the median is 1. It is 156 days old; check the official source for later updates before acting.
Shenzhen Langzhiyin Electronic Co.,Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Shenzhen Langzhiyin Electronic Co.,Ltd. | Shenzhen Guangdong, CN | 5 | 87th | 2026-06-02 |
| Inquis Medical, Inc. | Menlo Park, CA | 5 | 87th | 2026-10-16 |
| Boston Scientific Corp., Marina Bay Cust. Fulfillment Center | Quincy, MA | 6 | 88th | 2026-10-16 |
| Piraeus Medical, Inc. | Maple Grove, MN | 4 | 83rd | 2026-10-12 |
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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.