FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6
FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6 Q-switched Nd:YAG laser family.
$26,400
Hoya Con Bio Medlite C6 is a laser – yag from Hoya Con Bio. FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6 Q-switched Nd:YAG laser family.
Review technical facts, compatibility, included configuration and documentation before requesting a destination-specific B2B quotation.
Related products, categories and research.
Hoya Con Bio Medlite C6 is a laser – yag from Hoya Con Bio, identified by model/part reference Medlite C6. FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6 Q-switched Nd:YAG laser family.
Hoya Con Bio Medlite C6 is a laser – yag from Hoya Con Bio, identified by model/part reference Medlite C6. FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6 Q-switched Nd:YAG laser family.
For procurement, confirm the exact Hoya Con Bio Medlite C6 label or serial identification, compatibility, included accessories and configuration against the written offer before installation or clinical/technical deployment.
Match Hoya Con Bio Medlite C6 model/part and serial or product-label details to the quotation.
Review host-system, accessory, software, power and facility requirements where relevant.
Confirm condition, included items, warranty, documentation and delivery terms before payment.
Use the final quotation and exact-unit photographs to confirm the supplied configuration and condition.

These model-specific points help buyers evaluate identity, compatibility and purchasing requirements.
FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6 Q-switched Nd:YAG laser family.
Current Cynosure documentation continues the MedLite C6 product lineage after corporate ownership changes.
Verify exact handpieces, wavelengths/modes, software, cooling, pulse/spot options and regulatory labeling on the physical unit.
Final suitability depends on the exact model configuration, compatible systems, professional use requirements and manufacturer instructions.
Evaluate Hoya Con Bio Medlite C6 for procedures specifically supported by the exact model, wavelength, handpiece and manufacturer documentation.
Confirm application-specific accessories, consumables, cooling, power and safety requirements before use.
Useful where the exact laser platform and handpieces fit an established clinical or aesthetic workflow.
Laser classification, protective eyewear, plume control, training and local regulatory requirements should be reviewed before commissioning.
Use these details for product identification. Configuration-sensitive specifications should be checked against the exact supplied unit and manufacturer documentation.
Use this checklist to avoid configuration or compatibility mismatches.
Use authoritative documentation to confirm model identity, compatibility, operating requirements and configuration-sensitive details.
Technical or regulatory resource relevant to Hoya Con Bio Medlite C6 product evaluation.
Technical or regulatory resource relevant to Hoya Con Bio Medlite C6 product evaluation.
Key questions for evaluating Hoya Con Bio Medlite C6 before purchase.
Hoya Con Bio Medlite C6 is a laser – yag from Hoya Con Bio. FDA 510(k) K060977 explicitly identifies Hoya ConBio and the MedLite C6 Q-switched Nd:YAG laser family.
Exact laser model, wavelength/module configuration and serial number; Installed software and treatment modes; Handpieces/fibers/scanner/tips included.
No. Hardware revision, software, accessories, probes, handpieces, modules or other options can vary. The written quotation and exact-unit identification should define the supplied configuration.
Only items explicitly listed in the quotation and packing scope should be treated as included. Reference photographs may show accessories or system components that are not part of the final offer.
International B2B delivery can be arranged for approved destinations subject to product-specific transport requirements, customs rules and the agreed Incoterms, freight and insurance conditions.
Manufacturer names and trademarks are used for product identification. Confirm model-specific instructions, compatibility and regional requirements before use.
Model, label/serial information, condition and supplied configuration can be confirmed before dispatch.
Quotation, packing scope, warranty terms and delivery responsibilities are documented before order approval.
Export packing, freight, insurance and shipment documentation can be coordinated for approved destinations.
Support is available for configuration questions, installation planning and procurement documentation.
Include delivery country, quantity, required configuration and target purchase date for a destination-specific offer.
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