Supplier qualification and manufacturing evidence
AOVAPE Manufacturing & Quality Evidence
Review AOVAPE’s company identity, production environment, project controls and the documents buyers can request before approving a vape or vaporizer manufacturing program.
Company Identity
| Brand | AOVAPE |
|---|---|
| Founded | 2017 |
| Operating location | Shajing, Bao’an District, Shenzhen, Guangdong, China |
| Business focus | B2B vape and vaporizer hardware, existing-platform OEM, ODM and new-tooling development |
| Public trademark record | The official USPTO record lists Shenzhen Aoweipu Technology Co., Ltd. in connection with the AOVAPE mark, U.S. Registration No. 5941691. View the USPTO record. |
| Public incorporation reference | A public Hong Kong company directory records AOVAPE Technology Co., Limited as incorporated on 29 May 2017. View the directory record. |
Public links help buyers cross-check the brand and founding timeline. Current legal, banking and contracting entities should always be confirmed on the quotation and supplier documents used for the specific order.
Quality Controls Buyers Can Put in Writing
- Incoming material check: confirm the specified housing, cell, PCB, heater or cartridge components before assembly.
- Engineering and sample review: record fit, finish, controls, charging, output and compatibility observations against the brief.
- Golden-sample approval: retain the approved physical sample and written specification as the production reference.
- In-process inspection: check assembly and critical functions at agreed stages rather than relying only on finished-goods inspection.
- Final and pre-shipment review: inspect agreed appearance, function, quantity, packaging and traceability items before release.
Documents to Request for Your Specific Project
Company & Commercial
Current company registration, quotation entity, bank details, NDA, tooling-use terms and design-ownership agreement.
Product & Components
Approved specification, bill-of-material scope, component declarations and product-specific test or compliance reports where applicable.
Samples & Production
Sample revision record, golden-sample approval, inspection criteria, defect handling and agreed production checkpoints.
Shipping & After-Sales
Packing list, transport documents required for the product, traceability information and written handling of confirmed quality issues.
Compliance is product- and market-specific. AOVAPE does not treat one generic certificate as proof for every device or destination; the applicable reports are confirmed during quotation.
Published Project Evidence
The Shatterizer manufacturing case study documents a real supplier relationship. The DynaVap induction heater OEM/ODM project provides limited evidence of another custom cooperation. Although its initial five-year confidentiality period has passed, AOVAPE continues to withhold sensitive project details. Both pages separate project evidence from general marketing claims.
Supplier Qualification FAQ
Can AOVAPE provide every certificate shown on a generic factory website?
Documents depend on the exact device, battery, destination market and test scope. Ask AOVAPE to identify the report, model and issuing body that apply to your proposed product.
Can buyers request a factory or video review?
Contact AOVAPE with your supplier-qualification requirements. The team can confirm what current factory, video-call and project evidence can be provided for the inquiry.
How are design ownership and tooling handled?
NDA, design ownership, tooling payment, use rights, storage and maintenance should be stated in the project agreement before new-tooling work begins.
Qualify AOVAPE for Your Project
Send the product category, target market, expected volume and your supplier-document checklist. We will confirm the applicable company, product, test and production materials.