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Factory & Equipment
MedMoldPro is operated by C.K. MOLD & ENGINEERING LIMITED. Company information supplied for this website states that CKMOLD was established in 2002, has approximately 60 employees, operates more than 15 injection molding machines with capacity up to approximately 1200T, and supports DFM, mold design, CNC, EDM, wire cutting, mold trials, injection molding, and CMM inspection internally.
Suitable Projects
- Buyers evaluating tooling and molding under one organization
- Programs requiring internal mold manufacture and trials
- Parts needing machine selection across a broad size range
- Teams planning inspection and project communication before a visit
Engineering Risks to Resolve
- Matching the part and mold to an appropriate machine
- Coordinating design, machining, trial, correction, and molding
- Verifying equipment rather than relying on generic marketing claims
- Protecting confidential customer work during remote or on-site review
How MedMoldPro Approaches the Work
Facility and equipment suitability are confirmed during quotation for the actual mold and part.
For suitable projects, a typical T1 target is approximately 28–35 working days after 3D mold design approval, but complexity, steel, components, revisions, and test requirements can change timing.
Expected Project Deliverables
- Manufacturing-route confirmation
- Project schedule based on the approved scope
- Equipment and inspection suitability review
- Visit or evidence coordination subject to confidentiality and permission
Scope and Responsibility Boundary
No machine brand, exact machine count by tonnage, cleanroom, or certificate is claimed without current evidence. Existing customer work and facility images are not published without permission.
Factory & Equipment: Frequently Asked Questions
Company information supplied for this website states 2002.
Current company information states more than 15 machines, with project suitability confirmed during quotation.
No current scope-matched certificate was available in the website records reviewed, so this page does not make that claim.
A visit or remote evidence review can be discussed subject to scheduling, confidentiality, safety, and permission.
Technical review: Jerry Zou | Last updated: August 28, 2026
Manufacturing statements are limited to available capability information. Regulatory references are informational and do not replace the legal manufacturer’s qualified review.
Discuss the Drawing, Material, Volume, and Documentation Scope
Send the controlled files and project requirements needed for an engineering review and quotation.