Guangdong Carain Beauty Equipment Co., Ltd (contract manufacturer, Foshan Guangdong, CN): 3 new FDA device listings, incl. powered microneedle device

Guangdong Carain Beauty Equipment Co., Ltd (Foshan Guangdong): 3 new FDA device listings, incl. powered microneedle device. Its amount of 3 is above the median of 2 (77th percentile). Dated 29 days ago, it is in the active follow-up window. Score 80/100. As of 2026-11-04, 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 2,709 DeviceEstablishmentPulse records · 1.5x the median

Free preview: all 15 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentGuangdong Carain Beauty Equipment Co., Ltd
Owner / operatorGuangdong Carain Beauty Equipment
RoleContract manufacturer
Establishment typesManufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
LocationFoshan Guangdong, CN
New listings3
DevicesPowered Microneedle Device
Product codesQAI
Device classesClass II
Medical specialtiesGeneral, Plastic Surgery
Brand namesSER Pen Carain MicroSystem (Model MP1209SP); SkinStylus SteriLock® Cartridge Hilo ( SL38679);; SkinStylus SteriLock® Cartridge 36pin ( 10446);; SkinStylus SteriLock® Cartridge 12pin ( 10445);; SkinStylus SteriLock® Cartridge MicroSystem ( 4501)
First new listing2026-08-05
Latest new listing2026-10-07
FDA registration number3011568699
Registration expires2027-12-31
amount percentile77th of 2,709 (median 2, 1.5x 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: 2026-10-07
  • Data refreshed: 2026-11-04
  • 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, 04 Nov 2026 21:52:36 GMT

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Peer benchmark and outreach value: Guangdong Carain Beauty Equipment Co., Ltd and 720 CN peers

  • CN DeviceEstablishmentPulse records like this one: 720
  • Guangdong Carain Beauty Equipment Co., Ltd's amount: 77th percentile of 2,709 records
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every CN peer: $144,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Guangdong Carain Beauty Equipment Co., Ltd in Foshan Guangdong?

Guangdong Carain Beauty Equipment Co., Ltd (Foshan Guangdong, CN), a contract manufacturer, added 3 FDA device listings between 2026-08-05 and 2026-10-07.

How does Guangdong Carain Beauty Equipment Co., Ltd compare to other DeviceEstablishmentPulse records?

Its amount of 3 sits in the upper half (77th percentile) of 2,709 records; the median is 2. It is 29 days old, still within a typical 45-day follow-up window. Its Score of 80/100 puts it among the stronger signals in this feed.

Guangdong Carain Beauty Equipment Co., Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Guangdong Carain Beauty Equipment Co., LtdFoshan Guangdong, CN377th2026-10-07
Tecomet Inc.Wilmington, MA377th2026-10-15
Bard Shannon LimitedHumacao, PR377th2026-10-14
Orchid Orthopedic Solutions Oregon, Inc.Oregon City, OR377th2026-10-05

Related records

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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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