Neoconcepts LLC (other, Lewis Center, OH): 3 new FDA device listings, incl. low power electrosurgical devices for skin lesion destruction
Neoconcepts LLC (Lewis Center, Ohio): 3 new FDA device listings, incl. low power electrosurgical devices for skin lesion destruction. Its amount of 3 is above the median of 1 (77th percentile). Dated 85 days ago, it serves as a historical benchmark. Score 65/100. 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: 3 · 77th percentile of 2,570 DeviceEstablishmentPulse records · 3.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 41 related OH DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Neoconcepts LLC |
| Owner / operator | NEOconcepts LLC |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Lewis Center, OH, US |
| New listings | 3 |
| Devices | Low Power Electrosurgical Devices For Skin Lesion Destruction; Powered Microneedle Device; Electrosurgical, Cutting & Coagulation & Accessories |
| Product codes | QVJ, QAI, GEI |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | Prism Plasma; Exceed Unlimited; AgeJet |
| First new listing | 2026-08-12 |
| Latest new listing | 2026-08-12 |
| FDA registration number | 3015227849 |
| Registration expires | 2026-12-31 |
| amount percentile | 77th of 2,570 (median 1, 3.0x median) |
| Peer records CSV (42 OH 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: 2026-08-12
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (OH first): Sterigenics US, LLC (contract sterilizer, Lewis Center, OH) · Aps Materials, Inc. (contract manufacturer, Dayton, OH) · Health Care Logistics, Inc. (repackager or relabeler, Urbanc · Hammill Mfg. Co. (contract manufacturer, Maumee, OH) · Guardian Medical USA, Inc (contract manufacturer, Swanton, O · 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: Neoconcepts LLC and 42 Ohio peers
- Ohio DeviceEstablishmentPulse records like this one: 42
- Neoconcepts LLC's amount: 77th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Ohio peer: $8,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Neoconcepts LLC in Lewis Center, Ohio?
Neoconcepts LLC (Lewis Center, OH), a other, added 3 FDA device listings on 2026-08-12.
How does Neoconcepts LLC compare to other Ohio DeviceEstablishmentPulse records?
Its amount of 3 sits in the upper half (77th percentile) of 2,570 records; the median is 1. It is 85 days old; check the official source for later updates before acting.
Neoconcepts LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Neoconcepts LLC | Lewis Center, OH | 3 | 77th | 2026-08-12 |
| Conmed Corporation | Utica, NY | 3 | 77th | 2026-09-14 |
| Euroimmun Us Inc. | Mountain Lakes, NJ | 3 | 77th | 2026-09-10 |
| Rohrer Aesthetics, Inc. | Homewood, AL | 3 | 77th | 2026-09-09 |
Related records
DeviceEstablishmentPulse: Other DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Ohio
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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.