Data / Medical devices / China / Feellife Health Inc.
Feellife Health Inc.: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances
Feellife Health Inc. is registered with the FDA (registration 3014916466) in Shenzhen Guangdong, China. It lists 8 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 12, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3014916466
- Address
- Room 2501, 1903, 2002, Building A, No.9 Furong Road Tantou Community, Songgang Subdistrict, Bao'an District, Shenzhen Guangdong, China, 518104
- Owner or operator
- FEELLIFE HEALTH INC. (10058685)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- August 3, 2020
- Registered through
- 2026
- Brand names listed
- Adapter: ICU NA1, ICU NA2, ICU NAH1, ICU NAH2, Adult T-Piece, Air Flow Sensor, Medical Mesh Nebulizer AirICU Max+, AirICU Max+ ST, Medication Cup, Medicine Chamber Spacers-AeroTube 220; AeroTube Mask(Adult); AeroTube Mask(Child), Mini Nasal Inhalator, Mini Nasal Inhalator - Air Nose I; Air Nose II and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Ent | KCJ | 1 | Manufacturer | accessdata.fda.gov |
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Contract manufacturer | accessdata.fda.gov |
| Jig, Piston Cutting, Ent, Non-Sterile | NNO | 1 | Manufacturer | accessdata.fda.gov |
| Mouthpiece, Breathing | BYP | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| Pump, Nebulizer, Manual | EPN | 1 | Specification developer | accessdata.fda.gov |
| Spirometer, Diagnostic | BZG | 2 | Manufacturer | accessdata.fda.gov |
| Ventilator-Compatible Nebulizer | SFP | 2 | Manufacturer, Specification developer | 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 |
|---|---|---|---|---|---|---|
| March 12, 2026 | K251584 | Medical Mesh Nebulizer (AirICU Max+) | SFP | Substantially Equivalent | AIRICU, Inc. | accessdata.fda.gov |
| August 9, 2023 | K222443 | Air Smart Extra Spirometer | BZG | Substantially Equivalent | Feellife Health, Inc. | accessdata.fda.gov |
| September 27, 2020 | K182906 | Portable Mesh Nebulizer | CAF | Substantially Equivalent | Feellife Health, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Jig, Piston Cutting, Ent, Non-Sterile
- All makers of Spirometer, Diagnostic
- All makers of Pump, Nebulizer, Manual
- All makers of Applicator, Ent
- All makers of Mouthpiece, Breathing
- All makers of Nebulizer (Direct Patient Interface)
Updated March 12, 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.