Nova

F&P Nova Nasal (Nasal PAP Therapy Mask) - Fit Pack S/M/L SL A

Registry build 21.09.26
18manufacturers in China registered for this device type
8catalogue numbers in this listing
30510(k) clearances naming this product code
7recalls on this code

Who Else Makes It

Concentrated in Guangdong (8), Jiangsu (2), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code BZD
Manufacturer City Province Registered as Device types
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Suzhou Avon Textile Co., Ltd. Suzhou Jiangsu Contract manufacturer 12
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Respironics Medical Products (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Hunan Beyond Medical Technology Co., Ltd. Changsha Hunan Contract manufacturer 3
Shanghai Baron Technologies Co Ltd Shanghai Shanghai Contract manufacturer 3
BMC(Dongguan) Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Zhejiang Baron Technologies Co., Ltd. Pinghu Zhejiang Contract manufacturer 1
Modern Medical Equipment Manufacturing (Qing Yuan) Ltd Qing Yuan Guangdong Contract manufacturer 26
Shenzhen Sany Pioneer Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Resvent Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 6

Showing 12 of 18. All 18 manufacturers in China registered for Ventilator, Non-Continuous (Respirator)

Record

Regulatory record for Nova
Listed by Fisher & Paykel Healthcare, Ltd., New Zealand
FDA product code BZD
Device type Ventilator, Non-Continuous (Respirator)
Device class Class 2
Regulation 21 CFR 868.5905
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2025-09-15
Record revised 2026-01-27 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature -20 to 50 °C
Packaging Pack of 10

Catalogue Numbers

Catalogue numbers for Nova
Catalogue number Size Status
NVN1MA Medium In distribution
NVN1LSLA Large In distribution
NVN1SSLA Small In distribution
NVN1LA Large In distribution
NVN1SMLA S/M/L In distribution
NVN1SA Small In distribution
NVN1SMLSLA S/M/L In distribution
NVN1MSLA Medium In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DreamStation Respironics Inc. 386
DreamWear Respironics Inc. 183
REMstar System One 60 Series Respironics Inc. 163
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 152
DeVilbiss DeVilbiss Healthcare LLC. 136
Ventilator, Non-Continuous (Respirator) Hans Rudolph, Inc. 115
BiPAP System One 60 Series Respironics Inc. 105
Ventilator, Non-Continuous (Respirator) Salter Labs 85
BiTrac Select Pulmodyne Inc. 79
Yuwell Sleep Apnea Breathing Therapy Mask Suzhou Yuyue Medical Technology Co., Ltd. 76
AF541 Respironics Inc. 71
CPAP Masks Sunset Healthcare Solutions, Inc. 69

Showing 12 of 699. All products under Ventilator, Non-Continuous (Respirator)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243583 2025-06-18
K221436 2023-06-29
K223696 2023-05-17
K212371 2022-03-18
K200089 2020-06-02
K190713 2019-10-11
K173193 2018-08-08
K161686 2017-01-24
K161412 2017-01-18
K153505 2016-09-20
K130328 2013-06-05
K121597 2012-10-02
K120027 2012-02-23
K110316 2011-08-19
K103786 2011-03-24
K100011 2010-10-08
K094040 2010-04-27
K083832 2009-03-16
K081029 2008-09-12
K080209 2008-09-12
K063036 2006-12-22
K061236 2006-08-29
K050904 2005-05-25
K041900 2004-08-31
K040941 2004-06-10
K040506 2004-05-05
K033087 2004-01-14
K023670 2003-06-12
K023559 2003-06-12
K003894 2001-06-25

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.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-04-22 Class II Nonconforming Material/Component Fisher and Paykel Healthcare is recalling the ICON CPAP units because there is a potential power issue on certain ICON CPAP. These ICON CPAP units could potentially become inoperable, which would result in a lack of treatment to the patien 1,407 units 2013-10-18
2006-11-24 Not classified Other Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use.
In the event of a tab breaking off, it may enter the CPAP system air path and the
815,239 total for all models, all lots 2012-03-26
2006-11-24 Not classified Other Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use.
In the event of a tab breaking off, it may enter the CPAP system air path and the
815,239 total for all models, all lots 2012-03-26
2006-11-24 Not classified Other Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use.
In the event of a tab breaking off, it may enter the CPAP system air path and the
815,239 total for all models, all lots 2012-03-26
2006-11-24 Not classified Other Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use.
In the event of a tab breaking off, it may enter the CPAP system air path and the
815,239 total for all models, all lots 2012-03-26
2006-11-24 Not classified Other Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use.
In the event of a tab breaking off, it may enter the CPAP system air path and the
815,239 total for all models, all lots 2012-03-26
2006-11-24 Not classified Other Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use.
In the event of a tab breaking off, it may enter the CPAP system air path and the
815,239 total for all models, all lots 2012-03-26

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer