Platinum Focus Group Ltd. (foreign exporter, London London, City of, GB): 16 new FDA device listings, incl. catheter, urological

Platinum Focus Group Ltd. (London London, City of): 16 new FDA device listings, incl. catheter, urological. Its amount of 16 is top-decile (96th percentile of 2,709 records). Dated 50 days ago, it serves as a historical benchmark. Score 55/100. 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: 16 · 96th percentile of 2,709 DeviceEstablishmentPulse records · 8.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 70 related GB DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentPlatinum Focus Group Ltd.
RoleForeign exporter
Establishment typesExport Device to the United States But Perform No Other Operation on Device
LocationLondon London, City of, GB
New listings16
DevicesCatheter, Urological; Catheter, Retention Type, Balloon; Non-Coring (Huber) Needle; Orthosis, Lumbo-Sacral; Collector, Ostomy; Adaptor, Ureteral Catheter; Introducer, Catheter; Bandage, Cast; Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment; Syringe, Piston
Product codesKOD, EZL, PTI, IPY, EXB, EYI, DYB, ITG, HWE, FMF, EXF, MON, FGE, CCK, BYG
Device classesClass I, Class II
Medical specialtiesGastroenterology, Urology, General Hospital, Physical Medicine, Cardiovascular, General, Plastic Surgery, Anesthesiology
Brand namesinjectable infusion set; ORTHOSIS, LUMBO-SACRAL; Collector, ostomy; ADAPTOR, URETERAL CATHETER; Introducer, catheter; BANDAGE, CAST; NSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT; 510(k)
First new listing2026-05-08
Latest new listing2026-09-16
FDA registration number3030446844
Registration expires2026-12-31
amount percentile96th of 2,709 (median 2, 8.0x 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: 2026-09-16
  • 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: Platinum Focus Group Ltd. and 71 GB peers

  • GB DeviceEstablishmentPulse records like this one: 71
  • Platinum Focus Group Ltd.'s amount: 96th percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every GB peer: $14,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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55 / 100 Score

  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Platinum Focus Group Ltd. in London London, City of?

Platinum Focus Group Ltd. (London London, City of, GB), a foreign exporter, added 16 FDA device listings between 2026-05-08 and 2026-09-16.

How does Platinum Focus Group Ltd. compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 16 is 8.0x the median of 2 across 2,709 records. It is 50 days old; check the official source for later updates before acting.

Platinum Focus Group Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Platinum Focus Group Ltd.London London, City of, GB1696th2026-09-16
Makar Consulting PTY LtdBelrose New South Wales, AU2197th2026-10-16
Mka Medikal Ic Ve Dis Ticaret Sanayi Limited SirketiCankaya Ankara, TR992nd2026-10-17
Maya Medical Top Trade Ltd.Tsofit Central, IL2497th2026-10-21

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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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