Revive Regenerative Inc. (other, Nashua, NH): 4 new FDA device listings, incl. massager, vacuum, radio frequency induced heat
Revive Regenerative Inc. (Nashua, New Hampshire): 4 new FDA device listings, incl. massager, vacuum, radio frequency induced heat. Its amount of 4 is above the median of 1 (83rd percentile). Dated 75 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: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 11 related NH DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Revive Regenerative Inc. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Nashua, NH, US |
| New listings | 4 |
| Devices | Massager, Vacuum, Radio Frequency Induced Heat; Powered Laser Surgical Instrument |
| Product codes | PBX, GEX |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | NeoSculpt Plus; 1927nm Thulium Laser System,model:PZ-DJG75-01,PZ-DJG75-02; Diode Laser Therapy System; Fractional CO2 Laser Therapy System (FG900-S,FG900-S2,PhantomClear) |
| First new listing | 2026-06-09 |
| Latest new listing | 2026-08-21 |
| FDA registration number | 3038715747 |
| Registration expires | 2026-12-31 |
| amount percentile | 83th of 2,570 (median 1, 4.0x median) |
| Peer records CSV (12 NH 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: 2026-08-21
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (NH first): Venus Concept Inc. (manufacturer, Windham, NH) · Deka Research & Development Corp. (specification developer, · Symmetry Medical, Inc. - Manchester (contract manufacturer, · A.M. Surgical, Inc. (specification developer, Nashua, NH) · Millyard Advanced Medical Products LLC (manufacturer, Manche · 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: Revive Regenerative Inc. and 12 New Hampshire peers
- New Hampshire DeviceEstablishmentPulse records like this one: 12
- Revive Regenerative Inc.'s amount: 83rd percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every New Hampshire peer: $2,400 (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 Revive Regenerative Inc. in Nashua, New Hampshire?
Revive Regenerative Inc. (Nashua, NH), a other, added 4 FDA device listings between 2026-06-09 and 2026-08-21.
How does Revive Regenerative Inc. compare to other New Hampshire DeviceEstablishmentPulse records?
Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 75 days old; check the official source for later updates before acting.
Revive Regenerative Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Revive Regenerative Inc. | Nashua, NH | 4 | 83rd | 2026-08-21 |
| Merz North America, Inc. | Sturtevant, WI | 4 | 83rd | 2026-09-23 |
| Rapid Medical Inc. | Southlake, TX | 4 | 83rd | 2026-09-20 |
| Conmed Corporation | Utica, NY | 3 | 77th | 2026-09-14 |
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DeviceEstablishmentPulse: Other DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in New Hampshire
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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.