Model note · Nebulizer
Philips InnoSpire Go Mesh Nebulizer
InnoSpire Go is a small, battery powered vibrating mesh nebuliser for adults and children from 2 years, at home or in hospitals and clinics. A palladium nickel mesh vibrating at about 137 kHz turns liquid medicine into aerosol without a compressor, and it runs from a built in rechargeable battery. It was cleared against the Aerogen Aeroneb Go and uses a mouthpiece or two mask sizes.
The model
Maker, model and type.
- Maker
- Respironics Respiratory Drug Delivery (UK) Ltd (Philips)
- Model
- InnoSpire Go Mesh Nebulizer
- Device type
- Nebulizer
- Main document
- Open the public document
Key specifications
What the public record says.
| Item | Value | Source |
|---|---|---|
| Aerosol generator | Vibrating palladium nickel mesh, 137 kHz; continuous output during inhalation and exhalation | Source |
| Reservoir and nebulisation rate | 8 mL; above 0.45 mL/min | Source |
| Particle size (salbutamol 5 mg/2.5 mL, 30 L/min) | MMAD 3.90 um, GSD 2.02; fine particle fraction under 5 um 61.1% | Source |
| Power | Internal rechargeable battery; AC adapter 100 to 240 V, under 5 W when charging | Source |
| Size and weight | About 46 x 130 x 70 mm; under 130 g including battery | Source |
| Operating and storage conditions | Operating 5 to 40 C, 15 to 93% RH, 70 to 106 kPa; storage minus 25 to 70 C | Source |
| Masks | Large (99 mL internal volume) and medium for ages 2 to 5 (34 mL) | Source |
| Standards and clearance | ES 60601-1, IEC 60601-1-2:2014, IEC 60601-1-6, IEC 60601-1-11; K170853 (November 2017), predicate Aeroneb Go K081650; product code CAF | Source |
Recalls
Recalls.
This note lists no recalls. Check the FDA recall database for the latest record.
Safety
Safety warnings from the record.
- Cleared for children from 2 years and adults only; younger infants are outside the cleared population. Source
- Output runs continuously through inhalation and exhalation rather than being breath actuated, so treatment technique should follow the prescriber's advice. Source
- Do not confuse it with the larger InnoSpire compressor nebulisers, whose MAUDE records include fire and thermal codes under the same brand word. Source
Sources
Where this note comes from.
- FDA 510(k) K170853 summary, InnoSpire Go
- openFDA MAUDE problem counts, InnoSpire Go
- openFDA MAUDE problem counts, InnoSpire brand (all models)
Not covered: The Philips InnoSpire Go user manual was not opened, so LED indicator meanings, cleaning agents, mesh life and battery runtime are not included. No FDA recall names InnoSpire Go. MAUDE has about a dozen InnoSpire Go reports, too few for a real trend; the fire and thermal codes belong to other InnoSpire models.
BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.