Light Guide Optics International Ltd. (contract manufacturer, Livani Preilu Novads, LV): 2 new FDA device listings, incl. catheter, peripheral, atherectomy

Light Guide Optics International Ltd. (Livani Preilu Novads): 2 new FDA device listings, incl. catheter, peripheral, atherectomy. Its amount of 2 is above the median of 1 (69th percentile). Dated 75 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: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 1 related LV DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentLight Guide Optics International Ltd.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
LocationLivani Preilu Novads, LV
New listings2
DevicesCatheter, Peripheral, Atherectomy; Powered Laser Surgical Instrument
Product codesMCW, GEX
Device classesClass II
Medical specialtiesCardiovascular, General, Plastic Surgery
Brand names1.5mm RX catheter (Hydrophilic); 1.5mm RX catheter (non coated); 0.9mm RX catheter (Hydrophilic); 0.9mm RX catheter (non coated); CORONA Infinite Ring XSCF 600 1.6 US; Bare Fiber 400 T Luer Lock; CORONA 360 Fused 600 1.8 US; Rigid Infinite Ring HSC Probe 600 1.8 US
First new listing2026-07-28
Latest new listing2026-08-21
FDA registration number3012669557
Registration expires2026-12-31
amount percentile69th of 2,570 (median 1, 2.0x 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: 2026-08-21
  • 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: Light Guide Optics International Ltd. and 2 LV peers

  • LV DeviceEstablishmentPulse records like this one: 2
  • Light Guide Optics International Ltd.'s amount: 69th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every LV peer: $400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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55 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.

What is the DeviceEstablishmentPulse record for Light Guide Optics International Ltd. in Livani Preilu Novads?

Light Guide Optics International Ltd. (Livani Preilu Novads, LV), a contract manufacturer, added 2 FDA device listings between 2026-07-28 and 2026-08-21.

How does Light Guide Optics International Ltd. compare to other DeviceEstablishmentPulse records?

Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 75 days old; check the official source for later updates before acting.

Light Guide Optics International Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Light Guide Optics International Ltd.Livani Preilu Novads, LV269th2026-08-21
Tecomet Inc.Wilmington, MA377th2026-10-15
Bard Shannon LimitedHumacao, PR377th2026-10-14
Orchid Orthopedic Solutions Oregon, Inc.Oregon City, OR377th2026-10-05

Related records

DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign establishment

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✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

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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