Shenzhen Tph Technology Co., Ltd. (contract manufacturer, Shenzhen Guangdong, CN): 7 new FDA device listings, incl. pump, breast, powered
Shenzhen Tph Technology Co., Ltd. (Shenzhen Guangdong): 7 new FDA device listings, incl. pump, breast, powered. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 73 days ago, it serves as a historical benchmark. Score 70/100. As of 2026-10-28, 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: 7 · 90th percentile of 2,570 DeviceEstablishmentPulse records · 7.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Shenzhen Tph Technology Co., Ltd. |
| Owner / operator | Shenzhen TPH Technology Co., Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Shenzhen Guangdong, CN |
| New listings | 7 |
| Devices | Pump, Breast, Powered |
| Product codes | HGX |
| Device classes | Class II |
| Medical specialties | Obstetrics/Gynecology |
| Brand names | Mother's Nature W1 Warming Wearable Breast Pump; Wearable Breast Pump (Model S32(A)); Wearable Breast Pump (Model S39); Figaroo Elevate Wearable Breast Pump(Model S39); DiscreetDuo Flow Wearable Breast Pump (Model S3); Wearable Breast Pump (Model S21A); eufy Wearable Breast Pump (T600P, T6000, T6001, T6002, T6003, T6004, T6005, T6006, T6007,T6008, T6009); eufy Wearable Breast Pump E20 (T6060) |
| First new listing | 2026-05-22 |
| Latest new listing | 2026-08-24 |
| FDA registration number | 3016975995 |
| Registration expires | 2026-12-31 |
| amount percentile | 90th of 2,570 (median 1, 7.0x median) |
| Peer records CSV (500 CN records) | 🔒 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: 2026-08-24
- Data refreshed: 2026-10-28
- 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, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Shenzhen Tph Technology Co., Ltd. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Shenzhen Tph Technology Co., Ltd.'s amount: 90th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Shenzhen Tph Technology Co., Ltd. in Shenzhen Guangdong?
Shenzhen Tph Technology Co., Ltd. (Shenzhen Guangdong, CN), a contract manufacturer, added 7 FDA device listings between 2026-05-22 and 2026-08-24.
How does Shenzhen Tph Technology Co., Ltd. compare to other DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 7 is 7.0x the median of 1 across 2,570 records. It is 73 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Shenzhen Tph Technology Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Shenzhen Tph Technology Co., Ltd. | Shenzhen Guangdong, CN | 7 | 90th | 2026-08-24 |
| NGInstruments, Inc dba Avalign Cutting Instruments | Warsaw, IN | 4 | 83rd | 2026-10-16 |
| Cook Medical LLC | Bloomington, IN | 4 | 83rd | 2026-10-13 |
| Swiss-American CDMO,LLC | Carrollton, TX | 4 | 83rd | 2026-10-12 |
Related records
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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.