Data / Medical devices / Vietnam / Perfect Medical Industry (VN) Co., Ltd
Perfect Medical Industry (VN) Co., Ltd: FDA-registered device maker in Ho Chi Minh City, Vietnam, 1 510(k) clearance
Perfect Medical Industry (VN) Co., Ltd is registered with the FDA (registration 3012646696) in Ho Chi Minh City, Vietnam. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 12, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012646696
- Address
- Block D7/I, No. 1B Road, Vinh Loc Industrial Zone, Binh Tan Ward, Ho Chi Minh City, Vietnam, 70000
- Owner or operator
- PERFECT MEDICAL INDUSTRY (VN) CO., LTD (10092703)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- February 7, 2025
- Registered through
- 2026
- Brand names listed
- EXEL Disposable Syringe, EXEL Disposable Syringe with Needle, Exel Disposable Syringe, Exel Disposable Syringe with needle, PERFECT Sterile Disposable Syringe, PERFECT Sterile Disposable Syringe with Needle, PERFECT Sterile Disposable Syringe with Safety Needle
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| June 12, 2024 | K232950 | Sterile Disposable Syringe, Sterile Disposable Syringe with needle, Sterile Disposable Syringe with safety needle | FMF | Substantially Equivalent | Perfect Medical Industry (Vn) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Syringe, Antistick
Updated June 12, 2024. 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.