Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. (foreign exporter, FATIH Istanbul, TR): 4 new FDA device listings, incl. lenses, soft contact, daily wear

Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. (FATIH Istanbul): 4 new FDA device listings, incl. lenses, soft contact, daily wear. Its amount of 4 is above the median of 2 (83rd percentile). Dated 143 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: 4 · 83th percentile of 2,709 DeviceEstablishmentPulse records · 2.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 6 related TR DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentZumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti.
RoleForeign exporter
Establishment typesExport Device to the United States But Perform No Other Operation on Device
LocationFATIH Istanbul, TR
New listings4
DevicesLenses, Soft Contact, Daily Wear; Lens, Contact, (Disposable)
Product codesLPL, MVN
Device classesClass II
Medical specialtiesOphthalmic
Brand namesPROCLEAR, PROCLEAR TORIC, PROCLEAR MULTIFOCAL; PROCLEAR 1DAY, PROCLEAR XC
First new listing2026-06-16
Latest new listing2026-06-16
FDA registration number3036689755
Registration expires2026-12-31
amount percentile83th of 2,709 (median 2, 2.0x median)
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  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-06-16
  • Data refreshed: 2026-11-04
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Top DeviceEstablishmentPulse records (TR first): Cardimed Asia Medikal Sanayi Ve Ticaret Ltd Sti (foreign exp · Burak Global Ic Ve Dis Tic Ltd Sti (foreign exporter, Kocasi · Mka Medikal Ic Ve Dis Ticaret Sanayi Limited Sirketi (foreig · Mikron Makina Sanayi Ve Ticaret Ltd. Sti. (manufacturer, Ive · Titanlinks Logistics LLC (repackager or relabeler, Newark, D · Browse all by state and category →

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: Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. and 7 TR peers

  • TR DeviceEstablishmentPulse records like this one: 7
  • Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti.'s amount: 83rd percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every TR peer: $1,400 (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 Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. in FATIH Istanbul?

Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. (FATIH Istanbul, TR), a foreign exporter, added 4 FDA device listings on 2026-06-16.

How does Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. compare to other DeviceEstablishmentPulse records?

Its amount of 4 sits in the upper half (83th percentile) of 2,709 records; the median is 2. It is 143 days old; check the official source for later updates before acting.

Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. vs. top 3 peers

OrganizationLocationAmountPercentileRecord dateCompare
Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti.FATIH Istanbul, TR483rd2026-06-16This record
Imperial Optical, IncTown Of Mount Royal, Quebec, CA377th2026-10-22View record →
Kash Sales Inc.Richmond Hill Ontario, CA890th2026-10-16View record →
Mka Medikal Ic Ve Dis Ticaret Sanayi Limited SirketiCankaya Ankara, TR992nd2026-10-17Compare Zumrut Lens Saglik Hizm. Ve Optik Ur. Dis. Tic. Ltd. Sti. vs Mka Medikal Ic Ve Dis Ticaret Sanayi Limited Sirketi →

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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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