Inpro Technology Device Factory
Registered establishment in Weifang, Shandong, China. 1 device type, 2 clearances.
Inpro Technology Device Factory is a manufacturer holding a current FDA establishment registration. The registration covers Vinyl Patient Examination Glove. Its earliest product listing with the FDA dates from 2011.
1device type
2510(k) clearances
Registration
| Registered name | INPRO TECHNOLOGY DEVICE FACTORY |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3009512322 |
| FEI number | 3009512322 |
| Establishment type | Manufacturer |
Location
| City | Weifang |
|---|---|
| Province | Shandong |
| Address | No.10-1, Xingan Road East, Linqu |
| Postal code | 262600 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Vinyl Patient Examination Glove | Class 1 | Inpro, omnishield | 2011 | 72 |
Clearances
| Clearance | Decision date | Product code | Route | Held by |
|---|---|---|---|---|
| K160468 | 2016-06-23 | LYZ | Traditional | This company |
| K112610 | 2011-12-05 | LYZ | Traditional | This company |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
The manufacturer named here can complete this record.