FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional
FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional powered laser surgical instrument.
$6,000
Solta Medical Fraxel SR1500is a Laser – Erbium from Solta. FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional powered laser surgical instrument.
Review the model information, technical details, compatibility, included configuration and documentation before requesting a destination-specific B2B quotation.
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Solta Medical Fraxel SR1500 is a Laser – Erbium from Solta. FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional powered laser surgical instrument.
Solta Medical Fraxel SR1500 is a Laser – Erbium from Solta. FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional powered laser surgical instrument.
The FDA indication document specifies 1550 nm use for soft-tissue coagulation, resurfacing and listed dermatologic indications, with a 1925 nm component in the documented system configuration.
For procurement, match the exact model or part number, included accessories, configuration and condition to the written quotation before installation or deployment.
Match model, part number and serial or product-label details to the quotation.
Review system, accessory, software, power and facility requirements that apply to this product.
Confirm condition, included items, warranty, documentation and delivery terms before payment.
Use the product media and final exact-unit photographs to confirm configuration and condition before shipment.

The points below summarize model-specific information supported by manufacturer, regulatory or technical documentation.
FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional powered laser surgical instrument.
The FDA indication document specifies 1550 nm use for soft-tissue coagulation, resurfacing and listed dermatologic indications, with a 1925 nm component in the documented system configuration.
Verify exact SR1500 versus SR1500 Dual configuration, handpiece/software, treatment tip system and laser calibration.
Suitability depends on the exact configuration, compatible systems, intended professional use and manufacturer instructions.
Evaluate Solta Medical Fraxel SR1500 only for procedures supported by the exact wavelength, handpiece and manufacturer documentation.
Confirm application accessories, consumables, cooling, electrical and room requirements before commissioning.
Useful where the exact laser platform and handpieces fit an established professional workflow.
Confirm classification, protective eyewear, plume control, training and applicable local safety requirements.
The table summarizes confirmed model and technical information available from product records and technical documentation. Configuration-sensitive values should be checked against the exact supplied unit.
Use this checklist to reduce configuration, compatibility and acceptance problems.
Manufacturer and regulatory references are prioritized so buyers can verify identity, compatibility and configuration-sensitive information.
Technical or regulatory resource relevant to Solta Medical Fraxel SR1500 evaluation.
Key questions for evaluating Solta Medical Fraxel SR1500 before purchase.
FDA K091420 identifies the Fraxel re:store laser system, model SR1500, as a fractional powered laser surgical instrument.
Exact model/revision; Wavelength/output or RF generator label; Handpieces/electrodes/fibers included.
No. Hardware revision, software, accessories, modules, handpieces, probes 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 can 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 freight, insurance and delivery terms.
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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