ABrite Tech (Shanghai) Co., Ltd.
US Last updated 31 May 2026
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- Devices
- 6
- Registries
- GUDIDFDA
- FDA recalls
- 0
Catalogue
Mysmile LP211-BK-MS Ref LP211-BK-MS
Mysmile LP221-BK-MS Ref LP221-BK-MS
Mysmile LP211-WT-MS Ref LP211-WT-MS
Mysmile LP211-PK-MS Ref LP211-PK-MS
Mysmile LP221-PK-MS Ref LP221-PK-MS
Mysmile LP221-WT-MS Ref LP221-WT-MS
FDA establishments
- Abrite Tech (Shanghai) Co., Ltd Shanghai · CN FEI 3030047599
What ABrite Tech (Shanghai) Co., Ltd. makes
ABrite Tech (Shanghai) Co., Ltd. manufactures water jet flossers, including the Mysmile device line, designed for oral hygiene by using a stream of water to clean between teeth and along the gumline.
The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Frequently asked questions
What types of medical devices does ABrite Tech (Shanghai) Co., Ltd. primarily manufacture?
ABrite Tech (Shanghai) Co., Ltd. specializes in water jet flossers, such as the Mysmile device line. These devices use a stream of water to clean between teeth and along the gumline, helping maintain oral hygiene. The company focuses exclusively on this category of dental care products.
Where is ABrite Tech (Shanghai) Co., Ltd. based, and how does that affect its regulatory oversight?
ABrite Tech (Shanghai) Co., Ltd. is based in the United States. Since the company operates within the US market, its devices are subject to FDA regulations. The FDA’s Unique Device Identifier (UDI) database includes listings for these products, ensuring traceability and compliance tracking.
How are the devices manufactured by ABrite Tech (Shanghai) Co., Ltd. classified under medical device regulations?
The devices produced by ABrite Tech (Shanghai) Co., Ltd., such as the Mysmile water jet flossers, are classified as Class I medical devices. This classification is typically assigned to low-risk products where general controls (like good manufacturing practices) are sufficient for ensuring safety and performance. Class I devices often require less stringent premarket review compared to higher-risk categories.
Are ABrite Tech (Shanghai) Co., Ltd.’s devices listed in any regulatory registries, and why does this matter?
Yes, ABrite Tech’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is critical for tracking and identifying medical devices throughout their lifecycle, ensuring transparency in supply chains, improving patient safety, and facilitating compliance with regulatory requirements. Listing in the UDI database helps healthcare providers and regulators verify product authenticity and recall information efficiently.
Information
- Country
- US
- DUNS number
- 617704886