Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026270764

FEI Number

3026270764

Entity Name

DONGGUAN DINGFOO PLASTIC PRODUCTS CO., LTD.

City/State/Country

Dongguan Guangdong, CN

Establishment Address

No.7, Hengtang Songyuan Street,Tangxia Town, Dongguan City, Dongguan Guangdong 523710, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Dongguan Dingfoo Plastic Products Co., Ltd. (Owner Number: 10090357)

Owner / Operator Contact Address

No.7, Hengtang Songyuan Street,Tangxia Town, Dongguan City, Dongguan, CN-GD 523710, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MYHIXEL Ring Disinfectant DF2366,DF2367,DF2368,DF2369,DF2370,DF2371,DF2372,DF2373,DF2374,DF2375,DF2376,DF2377,DF2378,DF2379,DF2380, DF2297,DF2298,DF2299,DF2300,DF2301,DF2302,DF2303,DF2304,DF2305,DF2306,DF2307,DF2308, DF2309,DF2310,DF2311,DF2312,DF2313,DF2314,DF2315. DF2331,DF2332,DF2333,DF2334,DF2335,DF2336,DF2337,DF2338,DF2339,DF2340,DF2341,DF2342,DF2343,DF2344,DF2345,DF2346, DF2444,DF2445,DF2446,DF2447,DF2448,DF2449,DF2450,DF2451,DF2452,DF2453,DF2454,DF2455, DF2280,DF2281,DF2282,DF2283,DF2284,DF2285,DF2286,DF2287,DF2288,DF2289,DF2290,DF2291,DF2292,DF2293,DF2294,DF2295,DF2296, Lubricant DF2265,DF2266,DF2267,DF2268,DF2269,DF2270,DF2271,DF2272,DF2273,DF2274,DF2275,DF2276,DF2277,DF2278,DF2279, DF2407,DF2408,DF2409,DF2410,DF2411,DF2412, DF2413,DF2414,DF2415,DF2416. DF2363,DF2364,DF2365. DF2431, DF2432,DF2433,DF2434,DF2435,DF2436,DF2437,DF2438,DF2439,DF2440,DF2441,DF2442,DF2443, DF2381, DF2381,DF2382,DF2383,DF2384,DF2385,DF2386,DF2387,DF2388,DF2389,DF2390,DF2391,DF2392,DF2393,DF2394,DF2395, Maintenance fluid DF2417,DF2418,DF2419,DF2420,DF2421,DF2422,DF2423, DF2424,DF2425,DF2426,DF2427,DF2428,DF2429,DF2430, DF2347,DF2348,DF2349,DF2350,DF2351,DF2352,DF2353,DF2354,DF2355,DF2356,DF2357,DF2358,DF2359,DF2360,DF2361,DF2362, DF2396, DF2397,DF2398,DF2399,DF2400,DF2401,DF2402,DF2403,DF2404,DF2405,DF2406, DF2456,DF2457,DF2458,DF2459,DF2460,DF2461,DF2462,DF2463,DF2464,DF2465,DF2466,DF2467. Climax Spray DF2316,DF2317,DF2318,DF2319,DF2320,DF2321,DF2322,DF2323,DF2324,DF2325,DF2326,DF2327,DF2328,DF2329,DF2330,

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2024-09-13
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2024-03-17

Official Correspondent

youwei chen

US Agent Details

Raymone Ben Email: fdafel520@outlook.com Phone: (303) 7319873

Related Public Records

Same Entity

Dongguan Dingfoo Plastic Products Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026270764. Last updated year: 2026. Please use registration number 3026270764 when referencing this establishment in official correspondence.