Karl Storz Endoscopy-America, Inc. (other, El Segundo, CA): 17 new FDA device listings, incl. hysteroscope (and accessories)

Karl Storz Endoscopy-America, Inc. (El Segundo, California): 17 new FDA device listings, incl. hysteroscope (and accessories). Its amount of 17 is top-decile (96th percentile of 2,709 records). Dated 17 days ago, it is in the active follow-up window. Score 75/100. 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: 17 · 96th percentile of 2,709 DeviceEstablishmentPulse records · 8.5x the median

Free preview: all 15 published fields of this record are shown below. Locked: 309 related CA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentKarl Storz Endoscopy-America, Inc.
Owner / operatorKarl Storz Se & Co Kg
RoleOther
Establishment typesComplaint File Establishment per 21 CFR 820.198
LocationEl Segundo, CA, US
New listings17
DevicesHysteroscope (And Accessories); Endoscope, Neurological; Coagulator-Cutter, Endoscopic, Unipolar (And Accessories); Laryngoscope, Nasopharyngoscope; System, Irrigation, Urological; Nasopharyngoscope (Flexible Or Rigid); Pump, Portable, Aspiration (Manual Or Powered); Insufflator, Hysteroscopic; Arthroscope; Endoscopic Irrigation/Suction System
Product codesHIH, GWG, KNF, EQN, LJH, EOB, BTA, HIG, HRX, OCX, GCJ, OSV, HIF, OCZ
Device classesClass II
Medical specialtiesObstetrics/Gynecology, Neurology, Ear, Nose, Throat, Gastroenterology, Urology, General, Plastic Surgery, Orthopedic
Brand namesUNIDRIVE Select System; UNIDRIVE SIII System; KARL STORZ Flexible Video Neuro-Endoscope; SUPRALOOP; KARL STORZ Laryngoscopes and Accessories; ENDOMAT SELECT; Smart Smoke Evacuation; ENDOFLATOR +
First new listing2026-06-17
Latest new listing2026-10-19
FDA registration number3010202439
Registration expires2027-12-31
amount percentile96th of 2,709 (median 2, 8.5x 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: 2026-10-19
  • 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: Karl Storz Endoscopy-America, Inc. and 310 California peers

  • California DeviceEstablishmentPulse records like this one: 310
  • Karl Storz Endoscopy-America, Inc.'s amount: 96th percentile of 2,709 records
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every California peer: $62,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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75 / 100 Score

  • 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 Karl Storz Endoscopy-America, Inc. in El Segundo, California?

Karl Storz Endoscopy-America, Inc. (El Segundo, CA), a other, added 17 FDA device listings between 2026-06-17 and 2026-10-19.

How does Karl Storz Endoscopy-America, Inc. compare to other California DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 17 is 8.5x the median of 2 across 2,709 records. It is 17 days old, still within a typical 45-day follow-up window. Its Score of 75/100 puts it among the stronger signals in this feed.

Karl Storz Endoscopy-America, Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Karl Storz Endoscopy-America, Inc.El Segundo, CA1796th2026-10-19
Premium Plus Dental Supplies IncBrooklyn, NY1395th2026-10-21
Home Health Us IncorporatedSarasota, FL1294th2026-10-22
Premium Plus Dental Supplies IncBrooklyn, NY1294th2026-09-25

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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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