Shenzhen Kaiyan Medical Equipment Co., Ltd (contract manufacturer, Shenzhen Guangdong, CN): 12 new FDA device listings, incl. light based over the counter wrinkle reduction

Shenzhen Kaiyan Medical Equipment Co., Ltd (Shenzhen Guangdong): 12 new FDA device listings, incl. light based over the counter wrinkle reduction. Its amount of 12 is top-decile (95th percentile of 2,570 records). Dated 85 days ago, it serves as a historical benchmark. Score 70/100. 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: 12 · 95th percentile of 2,570 DeviceEstablishmentPulse records · 12.0x 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.

FieldValue
EstablishmentShenzhen Kaiyan Medical Equipment Co., Ltd
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device; Export Device to the United States But Perform No Other Operation on Device
LocationShenzhen Guangdong, CN
New listings12
DevicesLight Based Over The Counter Wrinkle Reduction; Stimulator, Transcutaneous Electrical, Aesthetic Purposes; Fat Reducing Low Level Laser; Lamp, Infrared, Therapeutic Heating; Over-The-Counter Powered Light Based Laser For Acne
Product codesOHS, NFO, OLI, ILY, OLP
Device classesClass II
Medical specialtiesGeneral, Plastic Surgery, Neurology, Physical Medicine
Brand namesmyLEDmask 2 (MJ-144); FACEGYM Pro Device (HD-109); AXRAH Full-Body Red Light Therapy Mat (Model: FLUX, PULSE, ARC); iRESTORE Sculpt LED Belt; Lumaflex BodyPro (ZLD-05); Lumaflex Essential (ZLD-05A); Lumaflex Panel; Lumaflex Essential Pro (ZLD-05A Pro)
First new listing2026-05-13
Latest new listing2026-08-12
FDA registration number3011644607
Registration expires2026-12-31
amount percentile95th of 2,570 (median 1, 12.0x 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: 2026-08-12
  • 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 Kaiyan Medical Equipment Co., Ltd and 687 CN peers

  • CN DeviceEstablishmentPulse records like this one: 687
  • Shenzhen Kaiyan Medical Equipment Co., Ltd's amount: 95th 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)

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70 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Shenzhen Kaiyan Medical Equipment Co., Ltd in Shenzhen Guangdong?

Shenzhen Kaiyan Medical Equipment Co., Ltd (Shenzhen Guangdong, CN), a contract manufacturer, added 12 FDA device listings between 2026-05-13 and 2026-08-12.

How does Shenzhen Kaiyan Medical Equipment Co., Ltd compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 12 is 12.0x the median of 1 across 2,570 records. It is 85 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.

Shenzhen Kaiyan Medical Equipment Co., Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Shenzhen Kaiyan Medical Equipment Co., LtdShenzhen Guangdong, CN1295th2026-08-12
Biopro, Inc.Port Huron, MI1194th2026-10-15
Arthrex, Inc.Ave Maria, FL1093rd2026-09-27
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16

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✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

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.

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