Data / Medical devices / China / Sichuan Qianli-Beoka Medical Technology Inc.
Sichuan Qianli-Beoka Medical Technology Inc.: FDA-registered device maker in Chengdu Sichuan, China, 2 510(k) clearances
Sichuan Qianli-Beoka Medical Technology Inc. is registered with the FDA (registration 3018455773) in Chengdu Sichuan, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 19, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018455773
- Address
- Longtan Industrial Park 2nd Sec, East 3rd Ring Road, Chenghua District, Chengdu Sichuan, China, 610052
- Owner or operator
- Sichuan Qianli-beoka Medical Technology Inc. (10091568)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- October 16, 2024
- Registered through
- 2026
- Brand names listed
- Air Compression Massager, Air compression massager models ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6, C2-D; CUTE X MAX-BK; CUTE X MAX-GR; CUTE X MAX-WH; CUTE X-A-CH; CUTE X-A-H; CUTE X1-BK; CUTE X1-GR; CUTE X1-RD;, CUTE X1-WH; CUTE X1-YW; D5 Pro-BK; D5 Pro-WH; D5-C; D6 Pro; Deep Muscle Massager; F5-A; Knee Massager;, CurrentBody Wellness Recovery Boots, MINI.A1-BK; MINI.A1-WH; Neck Massager; Q2-D; QL/A2-C; QL/D2-C; QL/DMS.C2-J; QL/DMS.C2-M; QL/DMS.C2-N; QL/DMS.Q2-F;, QL/DMS.T2-D; QL/DMS.T2-E; QL/DMS.T2-H; QL/DMS.X6-E; QL/DMS.X6-F; QL/DMS.X6-H; RP-GM171; RP-GM173; RP-GM180; S5Pro-A-CH;, QL/DMS.T2-G; D6 Pro-C; D6 Pro-H; D6 Pro-G; D6 Pro-F; D6 Pro-E; D5-F; D5-E; QL/A2-C; QL/A2-E; R3-C and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Powered Inflatable Tube | IRP | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 19, 2025 | K243206 | Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) | IRP | Substantially Equivalent | Sichuan Qianli-Beoka Medical Technology, Inc. | accessdata.fda.gov |
| October 8, 2024 | K241446 | Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) | IRP | Substantially Equivalent | Sichuan Qianii-Beoka Medical Technoiogy Lnc. | accessdata.fda.gov |
Compare with other makers
Updated February 19, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.