Data / Medical devices / China / Tung Hing Plastic & Metal(shenzhen) Co. Ltd.
Tung Hing Plastic & Metal(shenzhen) Co. Ltd.: FDA-registered device maker in LONGGANG DIST, SHENZHEN Guangdong, China, 1 510(k) clearance
Tung Hing Plastic & Metal(shenzhen) Co. Ltd. is registered with the FDA (registration 3003062321) in LONGGANG DIST, SHENZHEN Guangdong, China. It lists 15 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 26, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003062321
- Address
- Tung Hing Ind BLDG, 8 Fugao West RD, Gaoqiao Ind Area, Pingdi Subdistrict, LONGGANG DIST, SHENZHEN Guangdong, China, 518117
- Owner or operator
- TUNG HING PLASTICS MANUFACTORY, LTD. (9060559)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- January 8, 2004
- Registered through
- 2026
- Brand names listed
- 400462 VAL PACK PILLPAL/PILLBOX 6/72, 400850 PILLBOX AM/PM 4/144, 400858 HARMON AM/PM PILLBOX 4/144, 63204RA RITE AID EMB PR DISP 12/288, 67004 WKLY CLASSIC PILL PLNR SM 6/72, 67004HSB-A PAD PRINTED SMALL PILL BOX BLUE OVERSEAS, 67004HSG-A PAD PRINTED SMALL PILL BOX GREEN OVERSEAS, 67004HSN-A PAD PRINTED SMALL PILL BOX NATURAL OVERSEAS and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Elastic | FQM | 1 | Manufacturer | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Contract manufacturer | accessdata.fda.gov |
| Device, Acupressure | MVV | U | Manufacturer | accessdata.fda.gov |
| Dilator, Nasal | LWF | 1 | Contract manufacturer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Contract manufacturer | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Compression | MHW | 1 | Manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Contract manufacturer | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Pill Crusher/Cutter | OHY | 1 | Contract manufacturer | accessdata.fda.gov |
| Scraper, Tongue | LCN | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Manufacturer | accessdata.fda.gov |
| Sling, Arm | ILI | 1 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 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 |
|---|---|---|---|---|---|---|
| November 26, 2004 | K041766 | EZY-TRAVEL WRISTBAND | MVV | Substantially Equivalent | Apothecary Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Dispenser, Liquid Medication
- All makers of Dressing, Compression
- All makers of Massager, Therapeutic, Electric
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Device, Acupressure
- All makers of Toothbrush, Manual
Updated November 26, 2004. 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.