Data / Medical devices / China / Tianchang Jiarui Packaging Material Co., Ltd.
Tianchang Jiarui Packaging Material Co., Ltd.: FDA-registered device maker in Tianchang Anhui, China, 2 510(k) clearances
Tianchang Jiarui Packaging Material Co., Ltd. is registered with the FDA (registration 3013575574) in Tianchang Anhui, China. It lists 7 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 9, 2019. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013575574
- Address
- Yeshan Industria Zone, Tianchang Anhui, China, 239300
- Owner or operator
- Tianchang Jiarui Packaging Material Co., Ltd. (10054972)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- May 19, 2017
- Registered through
- 2026
- Brand names listed
- Dental Barrier and Sleeves, PeelVue Pro, barrier film, crepe paper, dental bibs, self sealing pouch, steam and EO indicator tapes, sterilization indicator tapes and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Absorber, Saliva, Paper | KHR | 1 | Manufacturer | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Manufacturer | accessdata.fda.gov |
| Holder, Film, X-Ray | EGZ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Indicator, Physical/Chemical Sterilization Process | JOJ | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Contract manufacturer | accessdata.fda.gov |
| Shield, Protective, Personnel | KPY | 1 | Manufacturer | accessdata.fda.gov |
| Wrap, Sterilization | FRG | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 9, 2019 | K181957 | Heat Sealing Sterilization Pouch Flat, Heat Sealing Sterilization Pouch Gusseted, Heat Sealing Sterilization Pouch Roll Flat, Heat Sealing Sterilization Pouch Roll Gusseted | FRG | Substantially Equivalent | Tianchang Jiarui Packaging Material Co., Ltd. | accessdata.fda.gov |
| April 28, 2017 | K162258 | Self Sealing Sterilization Pouches | FRG | Substantially Equivalent | Tianchang Jiarui Packaging Material Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mask, Surgical
- All makers of Shield, Protective, Personnel
- All makers of Absorber, Saliva, Paper
- All makers of Drape, Surgical, Exempt
- All makers of Indicator, Physical/Chemical Sterilization Process
- All makers of Wrap, Sterilization
Updated July 9, 2019. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.