Medinova Group Co. (manufacturer, Laguna Beach, CA): 21 new FDA device listings, incl. shield, eye, ophthalmic (including sunlamp protective eyewear and post

Medinova Group Co. (Laguna Beach, California): 21 new FDA device listings, incl. shield, eye, ophthalmic (including sunlamp protective eyewear and post. Its amount of 21 is top-decile (97th percentile of 2,570 records). Dated 179 days ago, it serves as a historical benchmark. Score 85/100. 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: 21 · 97th percentile of 2,570 DeviceEstablishmentPulse records · 21.0x the median

Free preview: all 13 published fields of this record are shown below. Locked: 283 related CA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentMedinova Group Co.
RoleManufacturer
Establishment typesComplaint File Establishment per 21 CFR 820.198; Manufacture Device in the United States for Export Only
LocationLaguna Beach, CA, US
New listings21
DevicesShield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear); Pad, Eye; Tape And Bandage, Adhesive; Applicator, Absorbent Tipped, Sterile; Disinfectant, Medical Devices; Container, Specimen Mailer And Storage, Non-Sterile; Dish, Tissue Culture; Punch, Gelfoam, Non-Sterile; Tray, Surgical, Instrument; Adhesive Backed Thermal Skin Patches
Product codesHOY, HMP, KGX, KXG, LRJ, NNK, KIZ, NNT, FSM, OMW, IMD, HTD, OEA, KEW, DJG
Device classesClass I, Class II
Medical specialtiesOphthalmic, General, Plastic Surgery, General Hospital, Pathology, Hematology, Ear, Nose, Throat, Physical Medicine, Clinical Toxicology, Microbiology
First new listing2026-05-09
Latest new listing2026-05-09
FDA registration number3044466317
Registration expires2026-12-31
amount percentile97th of 2,570 (median 1, 21.0x 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: 2026-05-09
  • 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: Medinova Group Co. and 284 California peers

  • California DeviceEstablishmentPulse records like this one: 284
  • Medinova Group Co.'s amount: 97th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every California peer: $56,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Medinova Group Co. in Laguna Beach, California?

Medinova Group Co. (Laguna Beach, CA), a manufacturer, added 21 FDA device listings on 2026-05-09.

How does Medinova Group Co. compare to other California DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 21 is 21.0x the median of 1 across 2,570 records. It is 179 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.

Medinova Group Co. vs. top 2 peers

OrganizationLocationAmountPercentileRecord date
Medinova Group Co.Laguna Beach, CA2197th2026-05-09
Inquis Medical, Inc.Menlo Park, CA587th2026-10-16
Endovascular Engineering, Inc.Menlo Park, CA377th2026-10-14

Related records

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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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