Data / Medical devices / United States / Revive Regenerative Inc.
Revive Regenerative Inc.: FDA-registered device maker in Nashua, NH, United States, 16 510(k) clearances
Revive Regenerative Inc. is registered with the FDA (registration 3038715747) in Nashua, NH, United States. It lists 7 device types. The FDA files 16 510(k) clearances under its listings, the newest dated April 3, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038715747
- Address
- 300 Innovative Way Ste 2235, Nashua, NH, United States, 03062
- Owner or operator
- Revive Regenerative Inc. (10093581)
- Roles
- Complaint file establishment
- First device listed
- August 1, 2025
- Registered through
- 2026
- Brand names listed
- 1927nm Thulium Laser System,model:PZ-DJG75-01,PZ-DJG75-02, APOLEX Tite, AgeJET, Avira, Colormax Pico, Colormax Plus, Diode Laser Therapy System, Emulsify and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Complaint file establishment | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Complaint file establishment | accessdata.fda.gov |
| Low Power Electrosurgical Devices For Skin Lesion Destruction | QVJ | 2 | Complaint file establishment | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 2 | Complaint file establishment | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Complaint file establishment | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Complaint file establishment | accessdata.fda.gov |
| System, Suction, Lipoplasty For Removal | QPB | 2 | Complaint file establishment | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 3, 2026 | K252495 | LSSA (NP-200) | QPB | Substantially Equivalent | Newpong Co., Ltd. | accessdata.fda.gov |
| March 9, 2026 | K252888 | NeoSculpt Plus | PBX | Substantially Equivalent | S&M Medical Co., Ltd. | accessdata.fda.gov |
| October 23, 2025 | K252732 | 1927nm Thulium Laser System (PZ-DJG75-01, PZ-DJG75-02) | GEX | Substantially Equivalent | Zhengzhou PZ Laser Slim Technology Co., Ltd. | accessdata.fda.gov |
| December 20, 2024 | K242688 | Finiff System | GEI | Substantially Equivalent | Skingrab Co., Ltd. | accessdata.fda.gov |
| December 20, 2024 | K241670 | Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2) | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| August 7, 2024 | K212969 | Liposaver | QPB | Substantially Equivalent | Lhbiomed Co., Ltd. | accessdata.fda.gov |
| June 12, 2024 | K233007 | Picosecond Nd:YAG Laser System; PICO LEGEND | GEX | Substantially Equivalent | Ami, Inc. | accessdata.fda.gov |
| February 20, 2024 | K233760 | Mjolnir Pro. (Multielectrode plasma) | QVJ | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| February 20, 2024 | K231896 | Diode Laser Therapy System | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| March 29, 2023 | K222485 | SMARTRION COMBI/Alexandrite & Long Pulsed Nd:YAG Laser | GEX | Substantially Equivalent | Ids, Limited | accessdata.fda.gov |
| March 21, 2023 | K222709 | Retraction, CWM-910T, APOLEX Tite | GEI | Substantially Equivalent | Chungwoo Co., Ltd. | accessdata.fda.gov |
| November 1, 2022 | K214090 | Back 3 COLOR | PBX | Substantially Equivalent | Swims America Corp | accessdata.fda.gov |
| July 7, 2022 | K212472 | AgeJet | GEI | Substantially Equivalent | Triworks Group Srl | accessdata.fda.gov |
| October 5, 2018 | K181868 | SHINY RPL System | ONF | Substantially Equivalent | Ids, Ltd. | accessdata.fda.gov |
| July 5, 2018 | K173359 | Fractional CO2 Surgical Laser System | GEX | Substantially Equivalent | Ami, Inc. | accessdata.fda.gov |
| December 7, 2017 | K172908 | Q-Switched Nd:YAG Laser System | GEX | Substantially Equivalent | Ami, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Low Power Electrosurgical Devices For Skin Lesion Destruction
- All makers of Massager, Vacuum, Radio Frequency Induced Heat
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Brush, Dermabrasion, Powered
Updated April 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.