Miniso Development Hong Kong Limited (repackager or relabeler, SAN PO KONG KL Hong Kong, CN): 6 new FDA device listings, incl. toothbrush, manual
Miniso Development Hong Kong Limited (SAN PO KONG KL Hong Kong): 6 new FDA device listings, incl. toothbrush, manual. Its amount of 6 is above the median of 2 (88th percentile). Dated 48 days ago, it serves as a historical benchmark. Score 40/100. As of 2026-11-04, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 6 · 88th percentile of 2,709 DeviceEstablishmentPulse records · 3.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Miniso Development Hong Kong Limited |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device; Export Device to the United States But Perform No Other Operation on Device |
| Location | SAN PO KONG KL Hong Kong, CN |
| New listings | 6 |
| Devices | Toothbrush, Manual; Tape And Bandage, Adhesive; Floss, Dental; Unit, Oral Irrigation; Dressing, Wound, Occlusive; Sunglasses (Non-Prescription Including Photosensitive) |
| Product codes | EFW, KGX, JES, EFS, NAD, HQY |
| Device classes | Class I |
| Medical specialties | Dental, General Hospital, General, Plastic Surgery, Ophthalmic |
| Brand names | Toothbrush; Band-Aids; Dental Floss; Blemish Patch; Sunglasses |
| First new listing | 2026-09-03 |
| Latest new listing | 2026-09-18 |
| FDA registration number | 3017833330 |
| Registration expires | 2026-12-31 |
| amount percentile | 88th of 2,709 (median 2, 3.0x median) |
| Peer records CSV (500 CN records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-09-18
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Miniso Development Hong Kong Limited and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Miniso Development Hong Kong Limited's amount: 88th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $144,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
40 / 100 Score
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Miniso Development Hong Kong Limited in SAN PO KONG KL Hong Kong?
Miniso Development Hong Kong Limited (SAN PO KONG KL Hong Kong, CN), a repackager or relabeler, added 6 FDA device listings between 2026-09-03 and 2026-09-18.
How does Miniso Development Hong Kong Limited compare to other DeviceEstablishmentPulse records?
Its amount of 6 sits in the upper half (88th percentile) of 2,709 records; the median is 2. It is 48 days old; check the official source for later updates before acting.
Miniso Development Hong Kong Limited vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Miniso Development Hong Kong Limited | SAN PO KONG KL Hong Kong, CN | 6 | 88th | 2026-09-18 |
| Uih Technologies, LLC | Houston, TX | 8 | 90th | 2026-10-21 |
| Tpc Advanced Technology, Inc. | City Industry, CA | 4 | 83rd | 2026-09-28 |
| Gurin Products LLC | Tustin, CA | 3 | 77th | 2026-10-22 |
Related records
DeviceEstablishmentPulse: Repackager or relabeler DeviceEstablishmentPulse: Foreign establishment
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.