Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Guangzhou Longest Science & Technology Co., Ltd. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
266 daysmedian FDA review time
783 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K202110 | MStim Drop Model: LGT-233 | Guangzhou Longest Science & Technology Co., Ltd. | 2021-11-05 | 463 | 0 |
| K201845 | Portable Electro-Stimulation Therapy Device, Model: LGT-232( | Guangzhou Longest Science & Technology Co., Ltd. | 2020-10-08 | 94 | 0 |
| K182020 | Portable Electro-Stimulation Therapy Device | Guangzhou Longest Science & Technology Co., Ltd. | 2020-09-17 | 783 | 0 |
| K191856 | Compression Therapy Device | Guangzhou Longest Science & Technology Co., Ltd. | 2020-03-19 | 252 | 0 |
| K191862 | Compression Therapy Device Model LGT-2200SP | Guangzhou Longest Science & Technology Co., Ltd. | 2019-10-29 | 110 | 0 |
| K182108 | Portable Electro-Stimulation Therapy Device | Guangzhou Longest Science & Technology Co., Ltd. | 2019-04-26 | 266 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda