Invia Motion 60 Days Npwt
The Invia Motion 60 Days pump provides negative pressure wound therapy for a single adult patient. It applies suction through a wound dressing and tubing to remove fluid into a collection…
The Invia Motion 60 Days pump provides negative pressure wound therapy for a single adult patient. It applies suction through a wound dressing and tubing to remove fluid into a collection canister. It is intended for use in hospitals, clinics, long-term care and home care.
A motor-driven membrane pump produces the suction. The user selects a pressure setting and continuous or intermittent operation. The portable pump runs from its rechargeable battery or AC power, and its display and audible signals communicate treatment status and faults.
Listed Item
Negative Pressure Wound Therapy Powered Suction Pump – 087.4024
Therapy Components
The 60 Days configuration has a limited operating runtime. The system uses a 150 mL canister and double-lumen tubing: one lumen carries wound fluid to the canister, while the smaller lumen supplies air flushing. The pump detects tubing blockage and gives visual and audible notifications.
Who Else Makes It
Concentrated in Jiangsu (4), Zhejiang (2), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Forefront Medical Technology (Jiangsu) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 14 |
| Alleva Medical (D.G.) Ltd | Dongguan | Guangdong | Contract manufacturer | 13 |
| Shanghai ISO Medical Products Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 8 |
| Zhejiang Longterm Medical Technology Co., Ltd. | Huzhou | Zhejiang | Contract manufacturer | 26 |
| VR Medical Technology Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 13 |
| Devon Medical Products (Jiangsu) Ltd | Nantong | Jiangsu | Repacker / relabeller | 12 |
| Nantong MedTech Medical Products Co., Ltd. | Nantong | Jiangsu | Contract manufacturer | 6 |
| Lightstone Medical Products (Ningbo) Co Ltd | Ningbo | Zhejiang | Specification developer | 3 |
Record
| Listed by | Medela LLC, United States |
|---|---|
| FDA product code | OMP |
| Device type | Negative Pressure Wound Therapy Powered Suction Pump |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4780 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| 510(k) | K161128 |
| Record published | 2024-08-22 |
| Record revised | 2024-12-16 (version 2) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 200.8591 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Cardinal Health | Cardinal Health 200, LLC | 57 |
| Pico | Smith & Nephew, Inc. | 57 |
| Negative Pressure Wound Therapy Powered Suction Pump | Carilex Medical, Inc. | 43 |
| DeRoyal | Deroyal Industries, Inc. | 34 |
| extriCARE | Oakwell Distribution, Inc. | 32 |
| Renasys | Smith & Nephew, Inc. | 27 |
| MicroDoc Npwt System | Pensar Medical | 26 |
| ExtriCARE | Alleva Medical Ltd | 22 |
| Vcare Alpha | I.V.T. Medical Ltd | 19 |
| V.A.C.® Granufoam™ | KCI USA, Inc. | 19 |
| Avance | Mölnlycke Health Care AB | 18 |
| Avance® Solo | Mölnlycke Health Care AB | 17 |
Showing 12 of 284. All products under Negative Pressure Wound Therapy Powered Suction Pump
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K223388 | 2023-07-07 |
| K214112 | 2022-07-26 |
| K182191 | 2019-02-01 |
| K180415 | 2018-11-02 |
| K172145 | 2018-05-09 |
| K170088 | 2017-04-06 |
| K161128 | 2016-12-01 |
| K151261 | 2015-10-07 |
| K142626 | 2015-06-12 |
| K141926 | 2014-12-19 |
| K113678 | 2012-10-01 |
| K080357 | 2008-07-24 |
| K061435 | 2006-06-08 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Medela LLC | 510(k) number | 2018-02-07 | Class II | Device Design | Device may display a battery missing error. | 778 units | 2018-12-04 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2019-12-02 | Class II | Packaging | Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging. | 331 | 2020-11-02 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.