Data / Medical devices / China / Shunde Lucas Industries
Shunde Lucas Industries: FDA-registered device maker in Foshan City Guangdong, China, 1 510(k) clearance
Shunde Lucas Industries is registered with the FDA (registration 9615551) in Foshan City Guangdong, China. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 10, 2014. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9615551
- FEI number
- 3003254346
- Address
- No.207-1, Liangxing Road Honggang Community, Daliang Sub-District, Shunde District, Foshan City Guangdong, China, 528300
- Owner or operator
- The Lucas Group (9035557)
- Roles
- Manufacturer
- First device listed
- November 10, 1998
- Registered through
- 2027
- Brand names listed
- Disposable Bedding, Disposable Surgical Apparel, MEGAMOVER ITEM NUMBER 51926, SHUNDE LUCAS, SHUNDE LUCAS HAND-CARRIED STRETCHER, SHUNDE LUCAS MANUAL PATIENT TRANSFER DEVICE, SHUNDE LUCAS Non-surgical isolation gown, SHUNDE LUCAS SURGICAL Dress and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Manufacturer | accessdata.fda.gov |
| Device, Transfer, Patient, Manual | FMR | 1 | Manufacturer | accessdata.fda.gov |
| Drape, Surgical, Antimicrobial | KKX | 2 | Manufacturer | accessdata.fda.gov |
| Dress, Surgical | FYE | 1 | Manufacturer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Manufacturer | accessdata.fda.gov |
| Stretcher, Hand-Carried | FPP | 1 | Manufacturer | accessdata.fda.gov |
| Suit, Surgical | FXO | 1 | Manufacturer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | 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 |
|---|---|---|---|---|---|---|
| September 10, 2014 | K140195 | SURGICAL DRAPE | KKX | Substantially Equivalent | Griffith-Lucas, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Gown, Examination
- All makers of Bedding, Disposable, Medical
- All makers of Accessory, Surgical Apparel
- All makers of Drape, Surgical, Antimicrobial
- All makers of Device, Transfer, Patient, Manual
- All makers of Stretcher, Hand-Carried
Updated September 10, 2014. 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.