Purebrand Slutions Ltd (foreign exporter, London England, GB): 71 new FDA device listings, incl. insufflator, laparoscopic

Purebrand Slutions Ltd (London England): 71 new FDA device listings, incl. insufflator, laparoscopic. Its amount of 71 is top-decile (99th percentile of 2,570 records). Dated 48 days ago, it serves as a historical benchmark. Score 55/100. 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: 71 · 99th percentile of 2,570 DeviceEstablishmentPulse records · 71.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 65 related GB DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentPurebrand Slutions Ltd
Owner / operatorPurebrand Solutions LTD
RoleForeign exporter
Establishment typesExport Device to the United States But Perform No Other Operation on Device
LocationLondon England, GB
New listings71
DevicesInsufflator, Laparoscopic; Laparoscope, General & Plastic Surgery; Knife, Ophthalmic; Cannula, Ophthalmic; Ligator, Esophageal; Container, Specimen, Sterile; Dilator, Catheter, Ureteral; Tubing, Noninvasive; Anoscope And Accessories; Audiometer
Product codesHIF, GCJ, HNN, HMX, MND, FMH, EZN, GAZ, FER, EWO, JOL, FRL, JOJ, BTO, FGE
Device classesClass I, Class II, Unclassified
Medical specialtiesObstetrics/Gynecology, Gastroenterology, Urology, Ophthalmic, Pathology, General Hospital, Ear, Nose, Throat, Anesthesiology, General, Plastic Surgery, Cardiovascular, Clinical Chemistry
Brand namesConmed Tri-Lumen Insufflator, laparoscopic; Beaver Visitec Knife, ophthalmic; Beaver Visitec Cannula, Ophthalmic; COOK-LIGATOR SAEED; BD TUBE, CONTAINER, VACUTAINER; COOK-DILATOR, CATHETER, URETERAL; Conmed Core tubing, noninvasive; Conmed AirSeal Insufflator, laparoscopic
First new listing2026-05-04
Latest new listing2026-09-17
FDA registration number3041276591
Registration expires2026-12-31
amount percentile99th of 2,570 (median 1, 71.0x 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: 2026-09-17
  • 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: Purebrand Slutions Ltd and 66 GB peers

  • GB DeviceEstablishmentPulse records like this one: 66
  • Purebrand Slutions Ltd's amount: 99th 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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55 / 100 Score

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

What is the DeviceEstablishmentPulse record for Purebrand Slutions Ltd in London England?

Purebrand Slutions Ltd (London England, GB), a foreign exporter, added 71 FDA device listings between 2026-05-04 and 2026-09-17.

How does Purebrand Slutions Ltd compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 71 is 71.0x the median of 1 across 2,570 records. It is 48 days old; check the official source for later updates before acting.

Purebrand Slutions Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord dateCompare
Purebrand Slutions LtdLondon England, GB7199th2026-09-17This record
Ad Supply Group LimitedLondon London, City of, GB3999th2026-10-13Compare Purebrand Slutions Ltd vs Ad Supply Group Limited →
Optikal (Southgate) LtdBorehamwood, GB377th2026-10-13View record →
Loudwater Trade Finance LtdLONDON England, GB377th2026-10-09View record →

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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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