Liaoning-Usa Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Liaoning-Usa Corp.” (first 1989, latest 1991), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 129 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LYY | Latex Patient Examination Glove | 2 | 2 |
| EFQ | Gauze/Sponge, Internal | 1 | 1 |
| FLK | Thermometer, Clinical Mercury | 1 | 1 |
| FYB | Gown, Patient | 1 | 1 |
| LDE | Stethoscope, Manual | 1 | 1 |
Review panels
Most recent Liaoning-Usa Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K911921 | DISPOSABLE ISOLATION GOWN | FYB | 1991-05-13 | 13 |
| K905487 | VARIOUS TYPES OF STETHOSCOPES | LDE | 1991-04-09 | 124 |
| K910623 | GAUZE SPONGES ABSORBENT GAUZE ROLLS | EFQ | 1991-04-01 | 47 |
| K902625 | CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT | FLK | 1990-10-26 | 134 |
| K892781 | ANTELOPE BRAND PATIENT EXAMINATION GLOVES | LYY | 1989-09-21 | 163 |
| K892774 | PATIENT EXAMINATION GLOVES | LYY | 1989-09-13 | 155 |
Recalls
openFDA lists no recalls under a recalling firm named Liaoning-Usa Corp..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Liaoning Upcera Co., Ltd. (10 510(k)s)
- Liaoning Kampo Medical System Co., Ltd. (1 510(k)s)
- Liaoning Rachcera Material Technology Co., Ltd. (1 510(k)s)
- Liaoning Shengjingtang Biotechnology Co., Ltd. (1 510(k)s)
- Liaoning Sidey Optoelectronics Technologies Co., Ltd. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Liaoning-Usa Corp.?
FDA lists 6 510(k) clearances under the applicant name “Liaoning-Usa Corp.” (first 1989, latest 1991), across 5 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Liaoning-Usa Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Liaoning-Usa Corp. is 129 days.
Which FDA product codes appear under Liaoning-Usa Corp.?
The most frequent FDA product codes under this applicant name are LYY (Latex Patient Examination Glove, 2); EFQ (Gauze/Sponge, Internal, 1); FLK (Thermometer, Clinical Mercury, 1).
Next steps
- See all 6 Liaoning-Usa Corp. clearances with predicates and recalls
- Run predicate analysis for product code LYY, Liaoning-Usa Corp.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.