Shanghai Jiawang Industrial Co. , Ltd.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Shanghai Jiawang Industrial Co. , Ltd.” (first 1997, latest 2003), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 39 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 |
|---|---|---|---|
| LYZ | Vinyl Patient Examination Glove | 4 | 4 |
| LZA | Polymer Patient Examination Glove | 1 | 1 |
Review panels
- General Hospital (5)
Most recent Shanghai Jiawang Industrial Co. , Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K032792 | PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW | LYZ | 2003-10-15 | 37 |
| K031854 | VINYL EXAM GLOVES, POWDER-FREE, YELLOW | LYZ | 2003-07-25 | 39 |
| K023428 | VINYL EXAMINATION GLOVE, POWDER-FREE, WHITE | LZA | 2002-10-25 | 14 |
| K970111 | JIAWANG POWDER-FREE VINYL EXAMINATION GLOVES | LYZ | 1997-03-27 | 73 |
| K964800 | JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES | LYZ | 1997-02-14 | 77 |
Recalls
openFDA lists no recalls under a recalling firm named Shanghai Jiawang Industrial Co. , Ltd..
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.
- Shanghai United Imaging Healthcare Co., Ltd. (85 510(k)s)
- Shanghai AnQing Medical Instrument Co., Ltd. (14 510(k)s)
- Shanghai Antares Industries, Inc. (14 510(k)s)
- Shanghai Apolo Medical Technology Co., Ltd. (14 510(k)s)
- Shanghai Palomar Mountain Industries, Inc. (12 510(k)s)
- Shanghai Sanyou Medical Co, Ltd. (9 510(k)s)
- Shanghai Chenguang Medical Technologies Co, Ltd. (8 510(k)s)
- Shanghai Motex Healthcare Co., Ltd. (8 510(k)s)
- Shanghai Poseidon Plastic Products Co., Ltd. (8 510(k)s)
- Shanghai Champion Plastic Products Co., Ltd. (6 510(k)s)
- Shanghai PT Plastics Enterprise Company, Ltd. (6 510(k)s)
- Shanghai SeeGen Photoelectric Technology Co., Ltd. (6 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Shanghai Jiawang Industrial Co. , Ltd.?
FDA lists 5 510(k) clearances under the applicant name “Shanghai Jiawang Industrial Co. , Ltd.” (first 1997, latest 2003), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Shanghai Jiawang Industrial Co. , Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Shanghai Jiawang Industrial Co. , Ltd. is 39 days.
Which FDA product codes appear under Shanghai Jiawang Industrial Co. , Ltd.?
The most frequent FDA product codes under this applicant name are LYZ (Vinyl Patient Examination Glove, 4); LZA (Polymer Patient Examination Glove, 1).
Next steps
- See all 5 Shanghai Jiawang Industrial Co. , Ltd. clearances with predicates and recalls
- Run predicate analysis for product code LYZ, Shanghai Jiawang Industrial Co. , Ltd.'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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.