Data / Medical devices / China / Foshan CICADA Dental Instrument Co., Ltd.
Foshan CICADA Dental Instrument Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 4 510(k) clearances
Foshan CICADA Dental Instrument Co., Ltd. is registered with the FDA (registration 3009768364) in Foshan Guangdong, China. It lists 15 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 11, 2022. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009768364
- Address
- B5-2F, Guangdong New Light Source Industrial Base, Shihan Town, Nanhai District Yanbu, Dali Town, Nanhai District, Foshan Guangdong, China, 528226
- Owner or operator
- FOSHAN CICADA DENTAL INSTRUMENT CO., LTD. (10051861)
- Roles
- Manufacturer
- First device listed
- July 4, 2016
- Registered through
- 2026
- Brand names listed
- Automatic Crown Remover, Crown Remover, CV/GX644, CV/GX652, CV/GX654, GK01L, GK02L, GK03L, GK45L, GN02L, GN45L, GN01, G401, G402, G445, G406, G408, G409, G410,, Curing Light, Broad Spectrum Curing Light, CV-215 G1--G8, 215i, 215i Plus, 216, 218, DTO, Dental Electric Motor: NL 400-1,NL 400-2,NL 400-3, NL 400-4, Disposable/Dental Irrigation Needle, Disposable/Dental Irrigation Syringe,, Endo Files, Dental Engine Files, Endo Hand Files, Endo Irrigation Tips, Disposable Endo Irrigation Tips, Endo Motor, Root Canal Motor Device T-Fine I, II, III, IV, V, VK-Endo I, II, III and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Activator, Ultraviolet, For Polymerization | EBZ | 2 | Manufacturer | accessdata.fda.gov |
| Controller, Foot, Handpiece And Cord | EBW | 1 | Manufacturer | accessdata.fda.gov |
| Epilator, High Frequency, Tweezer-Type | KCX | 1 | Manufacturer | accessdata.fda.gov |
| File, Bone, Surgical | EMI | 1 | Manufacturer | accessdata.fda.gov |
| File, Pulp Canal, Endodontic | EKS | 1 | Manufacturer | accessdata.fda.gov |
| Gutta-Percha | EKM | 1 | Manufacturer | accessdata.fda.gov |
| Handpiece, Air-Powered, Dental | EFB | 1 | Manufacturer | accessdata.fda.gov |
| Handpiece, Direct Drive, Ac-Powered | EKX | 1 | Manufacturer | accessdata.fda.gov |
| Knife, Surgical | EMF | 1 | Manufacturer | accessdata.fda.gov |
| Loupe, Diagnostic/Surgical | FSP | 1 | Manufacturer | accessdata.fda.gov |
| Microscope, Surgical | EPT | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Dental | DZM | 1 | Manufacturer | accessdata.fda.gov |
| Remover, Crown | EIS | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Periodontic, Endodontic, Irrigating | EIC | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Oral Irrigation | EFS | 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 |
|---|---|---|---|---|---|---|
| March 11, 2022 | K202075 | Dental Electric Motor | EBW | Substantially Equivalent | Foshan Cicada Dental Instrument Co, Ltd. | accessdata.fda.gov |
| March 12, 2021 | K192649 | Endo Motor | EKX | Substantially Equivalent | Foshan Cicada Dental Instrument Co, Ltd. | accessdata.fda.gov |
| February 13, 2020 | K192233 | LED Curing Light | EBZ | Substantially Equivalent | Foshan Cicada Dental Instrument Co, Ltd. | accessdata.fda.gov |
| December 9, 2019 | K181900 | Dental high speed handpiece, Dental low speed handpiece | EFB | Substantially Equivalent | Foshan Cicada Dental Instrument Co, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of File, Pulp Canal, Endodontic
- All makers of Unit, Oral Irrigation
- All makers of Syringe, Periodontic, Endodontic, Irrigating
- All makers of Handpiece, Air-Powered, Dental
- All makers of Gutta-Percha
- All makers of Knife, Surgical
Updated March 11, 2022. 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.