Invia Gauze Dressing Kit
The Invia Gauze Dressing Kit with FitPad is a single-use dressing kit for negative pressure wound therapy with the Invia Motion and Invia Liberty systems. Those therapy systems are used in…
The Invia Gauze Dressing Kit with FitPad is a single-use dressing kit for negative pressure wound therapy with the Invia Motion and Invia Liberty systems. Those therapy systems are used in acute, extended and home care settings. The kit must be used only with its approved therapy units.
The kit contains a gauze pad, transparent film, an Invia FitPad suction interface and saline. The gauze serves as the wound dressing material, while the tubing and suction interface connect the dressing to the negative pressure system.
Listed Item
Invia Gauze Dressing Kit with Fitpad – Medium 087.7170 3 pcs / 087.7172 15 pcs
Sterile Handling
Components are packaged sterile. Application uses clean, aseptic or sterile technique according to local protocol, and a kit should not be used if its sterile package has already been opened or damaged.
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) | K170088 |
| Record published | 2017-06-07 |
| Record revised | 2025-09-18 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Packaging | Pack of 3, pack of 15 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 200.8910 | In distribution | |
| 200.8909 | 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 | 2019-12-02 | Class II | Packaging | Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging. | 331 | 2020-11-02 |
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 |
|---|---|---|---|---|---|
| 2018-02-07 | Class II | Device Design | Device may display a battery missing error. | 778 units | 2018-12-04 |
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.