Amarigo Inc (manufacturer, Los Angeles, CA): 7 new FDA device listings, incl. pad, heating, powered

Amarigo Inc (Los Angeles, California): 7 new FDA device listings, incl. pad, heating, powered. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 41 days ago, it serves as a historical benchmark. Score 95/100. 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: 7 · 90th percentile of 2,570 DeviceEstablishmentPulse records · 7.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 283 related CA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentAmarigo Inc
RoleManufacturer
Establishment typesManufacture Medical Device
LocationLos Angeles, CA, US
New listings7
DevicesPad, Heating, Powered; Massager, Therapeutic, Electric; Spatula, Surgical, General & Plastic Surgery; Stimulator, Electrical, Non-Implantable, For Incontinence; Brush, Dermabrasion, Powered; Catheters, Suction, Tracheobronchial; Sunglasses (Non-Prescription Including Photosensitive)
Product codesIRT, ISA, GAF, KPI, GFE, BSY, HQY
Device classesClass I, Class II
Medical specialtiesPhysical Medicine, General, Plastic Surgery, Gastroenterology, Urology, Anesthesiology, Ophthalmic
Brand namesRechargeable heating pad:102409; Rechargeable massage waist protection:102385, HLX102247, 102319; Rechargeable Massage Elbow Guard:102415; Rechargeable Ankle Massager:102401, 102494; Rechargeable massage knee pads:HC-008, 102363; Rechargeable Massage Shoulder Support:102405, 102379, 102377, D10220009, KA506; Blackhead Remover:SL0001-1; Blackhead spatula:GUGU-FS-XK-VO3, BS-357
First new listing2026-05-18
Latest new listing2026-09-24
FDA registration number3027135885
Registration expires2026-12-31
amount percentile90th of 2,570 (median 1, 7.0x 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: 2026-09-24
  • 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: Amarigo Inc and 284 California peers

  • California DeviceEstablishmentPulse records like this one: 284
  • Amarigo Inc's amount: 90th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every California peer: $56,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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95 / 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.
  • U.S. establishment.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Amarigo Inc in Los Angeles, California?

Amarigo Inc (Los Angeles, CA), a manufacturer, added 7 FDA device listings between 2026-05-18 and 2026-09-24.

How does Amarigo Inc compare to other California DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 7 is 7.0x the median of 1 across 2,570 records. It is 41 days old, still within a typical 45-day follow-up window. Its Score of 95/100 puts it among the stronger signals in this feed.

Amarigo Inc vs. top 2 peers

OrganizationLocationAmountPercentileRecord date
Amarigo IncLos Angeles, CA790th2026-09-24
Inquis Medical, Inc.Menlo Park, CA587th2026-10-16
Endovascular Engineering, Inc.Menlo Park, CA377th2026-10-14

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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.

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