Probo Medical Ltd (foreign exporter, Gloucester Gloucestershire, GB): 19 new FDA device listings, incl. endoscopic video imaging system/component, gastroenterology-urology

Probo Medical Ltd (Gloucester Gloucestershire): 19 new FDA device listings, incl. endoscopic video imaging system/component, gastroenterology-urology. Its amount of 19 is top-decile (97th percentile of 2,570 records). Dated 43 days ago, it serves as a historical benchmark. Score 65/100. 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: 19 · 97th percentile of 2,570 DeviceEstablishmentPulse records · 19.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 65 related GB DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentProbo Medical Ltd
RoleForeign exporter
Establishment typesExport Device to the United States But Perform No Other Operation on Device
LocationGloucester Gloucestershire, GB
New listings19
DevicesEndoscopic Video Imaging System/Component, Gastroenterology-Urology; Transducer, Ultrasonic, Diagnostic; System, Imaging, Pulsed Echo, Ultrasonic; System, Imaging, Pulsed Doppler, Ultrasonic; Injector And Syringe, Angiographic; Full Field Digital, System, X-Ray, Mammographic; System, X-Ray, Tomography, Computed; Bronchoscope (Flexible Or Rigid); Endoscope, Accessories, Narrow Band Spectrum; System, Tomography, Computed, Emission
Product codesFET, ITX, IYO, IYN, DXT, MUE, JAK, EOQ, NWB, KPS, FAJ, OXO, JAA, OWB
Device classesClass II
Medical specialtiesGastroenterology, Urology, Radiology, Cardiovascular, Ear, Nose, Throat
Brand namesOlympus Camera Head; GE Voluson S10; Medrad Spectris Injector; GE Senographe Essential; Toshiba Aqulion; Olympus Processor; Siemens Biograph Horizon; GE Logiq E10
First new listing2026-05-06
Latest new listing2026-09-22
FDA registration number3010398867
Registration expires2026-12-31
amount percentile97th of 2,570 (median 1, 19.0x 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: 2026-09-22
  • 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: Probo Medical Ltd and 66 GB peers

  • GB DeviceEstablishmentPulse records like this one: 66
  • Probo Medical Ltd's amount: 97th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every GB peer: $13,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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65 / 100 Score

  • 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 Probo Medical Ltd in Gloucester Gloucestershire?

Probo Medical Ltd (Gloucester Gloucestershire, GB), a foreign exporter, added 19 FDA device listings between 2026-05-06 and 2026-09-22.

How does Probo Medical Ltd compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 19 is 19.0x the median of 1 across 2,570 records. It is 43 days old, still within a typical 45-day follow-up window.

Probo Medical Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Probo Medical LtdGloucester Gloucestershire, GB1997th2026-09-22
Optikal (Southgate) LtdBorehamwood, GB377th2026-10-13
Loudwater Trade Finance LtdLONDON England, GB377th2026-10-09
Ad Supply Group LimitedLondon London, City of, GB3999th2026-10-13

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DeviceEstablishmentPulse: Foreign exporter DeviceEstablishmentPulse: Foreign establishment

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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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