Data / Medical devices / New Zealand / Think Green Limited
Think Green Limited: FDA-registered device maker in Kumeu Auckland, New Zealand, 2 510(k) clearances
Think Green Limited is registered with the FDA (registration 3012684779) in Kumeu Auckland, New Zealand. It lists 12 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 19, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012684779
- Address
- 63 Riverland Road, Rd 2, Kumeu Auckland, New Zealand, 0892
- Owner or operator
- Think Green Limited (10052343)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- July 19, 2016
- Registered through
- 2026
- Brand names listed
- 75ml Silicone Milk Collector & Pump Combo(MHK160), 75ml Silicone Milk Collector Set and Silicone Pump Combo(AMZ039), Breastfeeding Nipple Shield - Orthodontic Teat (Round Base)(MHK083), Breastfeeding Nipple Shield - Orthodontic Teat (Triangle Base)(MHK082), Breastfeeding Nipple Shield - Round Base(MHK037), Breast Feeding Nipple Shield-Butterfly Shape(MHK038), Colostrum Essentials Pack - 4ml Collector (6pcs) + 750ml Steriliser Bag + Ice Brick(MHK208), Contoured Silicone Toothbrush(BHK121) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Holder, Syringe | IQG | 1 | Manufacturer | accessdata.fda.gov |
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Manufacturer | accessdata.fda.gov |
| Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure | PWA | 1 | Manufacturer | accessdata.fda.gov |
| Cup, Menstrual | HHE | 2 | Manufacturer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Breast, Non-Powered | HGY | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Breast, Powered | HGX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Ring, Teething, Non-Fluid Filled | MEF | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Nipple | HFS | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 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 19, 2024 | K242028 | Nasal Aspirator (BC-021, BC-022, BC-023, BC-024, BC-025, BC-026) | BTA | Substantially Equivalent | Dongguanshi Yiyingmei Technology Co., Ltd. | accessdata.fda.gov |
| January 20, 2022 | K212884 | Electric breast pump | HGX | Substantially Equivalent | Dongguan Rongfeng Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Irrigating (Non Dental)
- All makers of Adaptor, Holder, Syringe
- All makers of Toothbrush, Manual
- All makers of Pump, Breast, Powered
- All makers of Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure
- All makers of Shield, Nipple
Updated November 19, 2024. 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.