Data / Medical devices / China / Cao (china) Medical Equipment Company, Limited
Cao (china) Medical Equipment Company, Limited: FDA-registered device maker in Langfang, Hebei, China, 4 510(k) clearances
Cao (china) Medical Equipment Company, Limited is registered with the FDA (registration 3004475754) in Langfang, Hebei, China. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 11, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3004475754
- Address
- No. 19 Baihe Road Langfang Etdz, Langfang, Hebei, China, 065001
- Owner or operator
- CAO Group, Inc. (9043755)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 7, 2007
- Registered through
- 2026
- Brand names listed
- BlissBond, BlissEtch, FE Scrub Tip, FastFix, LEAP Cavity Cleansing Solution, Liqua Tip, Picasso Pro Diode Laser, Visco Tip
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Agent, Tooth Bonding, Resin | KLE | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Applicator, Resin | KXR | 1 | Contract manufacturer | accessdata.fda.gov |
| Heat Source For Bleaching Teeth | EEG | 1 | Manufacturer | accessdata.fda.gov |
| Laser, Dental, Soft Tissue | NVK | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Varnish, Cavity | LBH | 2 | 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 |
|---|---|---|---|---|---|---|
| March 11, 2026 | K254197 | Picasso Pro Diode Laser (002-00460) | GEX | Substantially Equivalent | CAO Group, Inc. | accessdata.fda.gov |
| October 21, 2009 | K092616 | ASCENT BOND UNIVERSAL ADHESIVE SYSTEM, MODELS 006-00029, 006-00030, 006-00044, 006-00045 | KLE | Substantially Equivalent | CAO Group, Inc. | accessdata.fda.gov |
| July 23, 2009 | K091300 | ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079 | KLE | Substantially Equivalent | CAO Group, Inc. | accessdata.fda.gov |
| May 25, 2007 | K070070 | ASCENT DENTAL CLEANSER | LBH | Substantially Equivalent | CAO Group, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Varnish, Cavity
- All makers of Agent, Tooth Bonding, Resin
- All makers of Laser, Dental, Soft Tissue
- All makers of Heat Source For Bleaching Teeth
- All makers of Powered Laser Surgical Instrument
- All makers of Applicator, Resin
Updated March 11, 2026. 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.