Wondview

25-Strip; Strep A Throat Swab Test

Registry build 21.09.26
6manufacturers in China registered for this device type
1catalogue number
5recalls on this code

Who Else Makes It

Concentrated in Zhejiang (3), Guangdong (1), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GTY
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Abon Biopharm (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 17
Hangzhou AllTest Biotech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 48
Guangzhou Wondfo Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 44
Jiangsu Macro & Micro-Test MED-Tech Co., Ltd. Nantong Jiangsu Manufacturer 11
BD Rapid Diagnostics (Suzhou) Co., Ltd. China (Jiangsu) Pilot Free Trade Zone Suzhou Area Manufacturer 6

Record

Regulatory record for Wondview
Listed by Wondfo USA Co., Ltd., United States
FDA product code GTY
Device type Antigens, All Groups, Streptococcus Spp.
Device class Class 1
Regulation 21 CFR 866.3740
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
510(k) K133343
Record published 2018-12-12
Record revised 2024-10-14 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Handling environment temperature 4 to 30 °C
Packaging Pack of 20

Catalogue Numbers

Catalogue numbers for Wondview
Catalogue number Size Per pack Status
W39-S 25 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
McKesson Mckesson Medical-Surgical Inc. 5
Sofia Quidel Corp. 4
QuickVue Quidel Corp. 4
Cardinal Health Cardinal Health 200, LLC 3
Strepaim Germaine Laboratories, Inc. 3
Rapid Response Btnx Inc. 3
Status Strep A Flip Princeton BioMeditech Corp. 3
Henry Schein Henry Schein, Inc. 3
Icon Beckman Coulter, Inc. 2
Poly stat Polymedco, Inc. 2
Group B Streptococcus Detection Kit(Immunochromatography) Jiangsu Macro & Micro-Test MED-Tech Co., Ltd. 2
Status Strep A Plus Princeton BioMeditech Corp. 2

Showing 12 of 148. All products under Antigens, All Groups, Streptococcus Spp.

Recalls

5 of these are Class II. Class II means a temporary or reversible health consequence. 5 are recorded with the root cause “No Marketing Application”: the device was distributed without the premarket submission its class requires, a compliance finding rather than a defect. 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
2024-04-22 Class II No Marketing Application Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or 170,000 units
2024-04-22 Class II No Marketing Application Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or 75,000 units
2024-04-22 Class II No Marketing Application Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or
2024-04-22 Class II No Marketing Application Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or 1,238,755 units
2024-04-22 Class II No Marketing Application Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home use, non-prescription use, over-the-counter use, or 102,500 units

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