Lens orders are placed by model number, diopter power and purchase order number. All prices are F.O.B. Clearwater, Florida.
BECOME A DISTRIBUTOR
Private labeling is available. Please contact a customer service representative for additional branding information or to find a distributor serving your geographic area.
RETURN OF GOODS POLICY
Unopened products can be exchanged for comparable dollar value provided they have not exceeded their expiration date. The returned product must be in their original, unopened, and undamaged packaging to be eligible for replacement or credit. A processing fee may be assessed for the unopened lenses. Prior to returning the lenses, a RETURN AUTHORIZATION NUMBER must be obtained from the Customer Service Department.
DO NOT ATTEMPT TO RESTERILIZE LENSES AND/OR PRODUCT!
A-CONSTANTS “A” – Constants shown are estimates. Values may be used as guidelines in the calculation of implant power. EyeKon recommends surgeons to develop their own values based on experience, technique, measuring equipment and desired postoperative results. CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN.
Registration
Register our products with our USA manufacturing facility, or our affiliated company located in the UK “EyeKon Medical, Ltd.”
EyeKon is an FDA Approved facility with products currently marketed in the United States and in over 100 countries worldwide. We received our first FDA Approval with the PMMA Posterior Chamber Intraocular Lens in 1985.
Certificates Include:
- ISO 13485
- CE Marked
- Declaration of Conformity
- Certificate to Foreign Government
- Certificate of Exportability