Manufacturer registered with FDA
Foshan Zike Technology Co., Ltd.
Foshan, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1China
Devices listed with FDA
What Foshan Zike Technology Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Air and/or Water Syringe UnitECB · Class 1 | Dental hand instruments | Maker | Air pressure suit:ZK-A01,ZK-A02,ZK-A03,ZK-A04,ZK-A05,ZK-A06,ZK-A07,ZK-A08,ZK-A09,ZK-A10,ZK-A11,ZK-A12,ZK-A13,ZK-A14,ZK-A15,ZK-A16,ZK-A17,ZK-A18,ZK-A19,ZK-A20 | 2026 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| FOSHAN ZIKE TECHNOLOGY CO., LTD.FDA reg. 3040278125 | Foshan Guangdong, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10094939). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.