FDA 注册服务
 
FDA）是一个在美国负责确保一部分消费品安全的监管机构。无论是在美国本土还是海外，任何食品、药品及医疗器械想要进入美国市场，其生产或销售公司都需要在FDA进行注册。一般用途眼镜产品（如配光眼镜，老花眼镜及非处方太阳镜）属医疗器械分类的1类产品，接受FDA监管。 
FDA注册流程
 
与PEL签订FDA注册代理合同
在FDA创建贵司账户并获取付款识别码
支付官费给FDA并获取付款确认码
PEL驻美代理人和官方发言人全权负责与FDA沟通与回应并获取所有者编码。
FDA注册完成，注册码公布 
 
精科眼镜检测检验服务有限公司是你最佳选择， PEL专业及经验丰富的技术人员可以给你提供有关FDA法规、注册及测试要求等最贴心的专业指导，给你最准确的预算评估，以最合理的价格及时限，提供最优质的服务！
 
FDA Registration services
The Food and Drug Administration (FDA) is a regulatory agency in the United States which is responsible for ensuring the safety of an array of consumer products. Both domestic and imported food, drug and medical devices to USA are mandatory to register under FDA regulation by law. Eyewear products for general use, such as reading glasses, ophthalmic lenses and non-prescription sunglasses, are classified as medical devices Class I, that are regulated by U.S. Food and Drug Administration.
 
FDA Regitration Workflow
1. Sign FDA registration contract with PEL
2. Establish the company account in FDA and obtain Personal Identification Number (PIN) from FDA.
3. Pay the official fee to FDA and obtain Payment Confirmation Number (PCN) from FDA.
4. FDA agent and official representative are responsible for all communication and feedback with FDA, Owner Number is obtained.
5. Completion of Registration, Registration Number posted in FDA official website.
 
PEL is your best preferable testing service provider when you do business to US market. Our dedicated and experienced consultants can provide you professional advices and guidelines in US FDA regulations, FDA registration or impact resistance test requirements / declaration. PEL provides quality service at a reasonable cost within a prompt lead time.