Omec Medical NV Inc (manufacturer, Reno, NV): 2 new FDA device listings, incl. speculum, rectal
Omec Medical NV Inc (Reno, Nevada): 2 new FDA device listings, incl. speculum, rectal. Its amount of 2 is above the median of 1 (69th percentile). Dated 120 days ago, it serves as a historical benchmark. Score 70/100. 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 15 published fields of this record are shown below. Locked: 9 related NV DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Omec Medical NV Inc |
| Owner / operator | OMEC Medical NV Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Reno, NV, US |
| New listings | 2 |
| Devices | Speculum, Rectal; Laparoscope, General & Plastic Surgery |
| Product codes | FFQ, GCJ |
| Device classes | Class I, Class II |
| Medical specialties | Gastroenterology, Urology |
| Brand names | Thermora Anoscope; 690 Laparoscope, 10 mm, 0 deg, 33 cm; 690 Laparoscope, 5.4 mm, 0 deg, 30 cm; 690 Laparoscope, 10 mm, 30 deg, 33 cm; 690 Laparoscope, 5.4 mm, 30 deg, 30 cm |
| First new listing | 2026-07-08 |
| Latest new listing | 2026-07-08 |
| FDA registration number | 3020142503 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (10 NV records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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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: 2026-07-08
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (NV first): Merits Health Products, Inc. (contract manufacturer, Las Veg · Medicreations LLC (repackager or relabeler, Las Vegas, NV) · Eiger Diagnostics, Inc. (manufacturer, Las Vegas, NV) · Restore Robotics Repairs LLC (remanufacturer, Henderson, NV) · Paragon Implant Company, LLC (manufacturer, Las Vegas, NV) · 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, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Omec Medical NV Inc and 10 Nevada peers
- Nevada DeviceEstablishmentPulse records like this one: 10
- Omec Medical NV Inc's amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Nevada peer: $2,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Omec Medical NV Inc in Reno, Nevada?
Omec Medical NV Inc (Reno, NV), a manufacturer, added 2 FDA device listings on 2026-07-08.
How does Omec Medical NV Inc compare to other Nevada DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 120 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Omec Medical NV Inc vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Omec Medical NV Inc | Reno, NV | 2 | 69th | 2026-07-08 |
| Beacon Biosignals, Inc. | Boston, MA | 3 | 77th | 2026-10-16 |
| Endovascular Engineering, Inc. | Menlo Park, CA | 3 | 77th | 2026-10-14 |
| INNO Holdings Inc. | Millcreek, UT | 3 | 77th | 2026-10-05 |
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.