Reference Source

Suqian Bing De Biotechnology Co. · 89-08 · CHINA

For Suqian Bing De Biotechnology Co., import alert is 89-08; country is CHINA; import alert name is "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"; product is Anti Snore Chin Strap | Anti Snore Chin Strap; product code is 76 L - - QZ Device, Jaw Repositioning | 76 L - - RK Device, Anti-Snoring; date published is 05/24/2016; address is Xu Ning Road, Si Hong County , Su Qian, Jiangsu CHINA, verified against its source on 2026-09-30.

Firm
Suqian Bing De Biotechnology Co. verified
Import alert
89-08
Import alert name
"Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"
Country
CHINA verified
Address
Xu Ning Road, Si Hong County , Su Qian, Jiangsu CHINA verified
Date published
05/24/2016 verified
Product code
76 L - - QZ Device, Jaw Repositioning | 76 L - - RK Device, Anti-Snoring each item verified
Product
Anti Snore Chin Strap | Anti Snore Chin Strap each item verified
FDA notes
Products do not have a valid 510(K) clearance. | Products do not have a valid 510(K) clearance. each item verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

Suqian Bing De Biotechnology Co. Date Published : 05/24/2016 Xu Ning Road, Si Hong County , Su Qian, Jiangsu CHINA

— accessdata.fda.gov, retrieved 2026-09-15

Where each value comes from

The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.

Product code, Product and FDA notes

76 L - - QZ Device, Jaw Repositioning Date Published: 05/24/2016 Desc: Anti Snore Chin Strap Notes: Products do not have a valid 510(K) clearance. 76 L - - RK Device, Anti-Snoring Date Published: 05/24/2016 Desc: Anti Snore Chin Strap Notes: Products do not have a valid 510(K) clearance.

— all from accessdata.fda.gov, retrieved 2026-09-15

Source

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