Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Shenzhen TPH Technology with 24 510(k) clearances. The most recent is a 510(k) clearance dated Sep 17, 2026: Wearable Breast Pump (Model S36).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 17, 2026 | Wearable Breast Pump (Model S36)K254203 · HGX | 510(k) clearances |
| Jul 24, 2026 | DiscreetDuo™ Flow Wearable Breast Pump (Model S3)K260259 · HGX | 510(k) clearances |
| Jul 13, 2026 | Wearable Breast Pump (Model S32A)K261199 · HGX | 510(k) clearances |
| Jun 9, 2026 | Mother's Nature W1 Warming Wearable Breast PumpK260864 · HGX | 510(k) clearances |
| May 21, 2026 | Wearable Breast Pump (Model S39)K254244 · HGX | 510(k) clearances |
| Apr 8, 2026 | Wearable Breast Pump (Model S21A)K260033 · HGX | 510(k) clearances |
| Feb 13, 2026 | Wearable Breast Pump (Model W2)K252422 · HGX | 510(k) clearances |
| Feb 13, 2026 | Wearable Breast Pump (Model W12)K252420 · HGX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
