Ulthera
Ulthera is a focused ultrasound aesthetic system from Ulthera, identified by model/part reference Ulthera. FDA K121700 identifies the Ulthera System as an aesthetic focused-ultrasound device platform.
Ulthera product information
Ulthera is a focused ultrasound aesthetic system from Ulthera, identified by model/part reference Ulthera. FDA K121700 identifies the Ulthera System as an aesthetic focused-ultrasound device platform.
For procurement, confirm the exact Ulthera label or serial identification, compatibility, included accessories and configuration against the written offer before installation or clinical/technical deployment.
Procurement focus
Match Ulthera 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.
Ulthera images
Use the final quotation and exact-unit photographs to confirm the supplied configuration and condition.
Important Ulthera details
These model-specific points help buyers evaluate identity, compatibility and purchasing requirements.
FDA K121700 identifies the Ulthera System as an aesthetic focused-ultrasound
FDA K121700 identifies the Ulthera System as an aesthetic focused-ultrasound device platform.
Ultherapy instructions for use describe imaging-plus-treatment architecture
Ultherapy instructions for use describe imaging-plus-treatment architecture and model-specific transducers.
Verify console/software, DeepSEE imaging function, treatment transducers
Verify console/software, DeepSEE imaging function, treatment transducers, shot counts/service status and regulatory labeling.
Where Ulthera can fit
Final suitability depends on the exact model configuration, compatible systems, professional use requirements and manufacturer instructions.
Diagnostic ultrasound
Designed for professional ultrasound imaging workflows according to the installed probes, software and model configuration.
Department deployment
Evaluate for radiology, point-of-care or specialty imaging workflows that match the documented configuration.
Fleet replacement or expansion
Can be assessed alongside existing ultrasound systems when probe, software, networking and accessory compatibility are confirmed.
Procurement projects
Suitable for hospital, clinic and imaging-center purchasing projects after exact configuration and site requirements are approved.
Ulthera specifications and identification
Use these details for product identification. Configuration-sensitive specifications should be checked against the exact supplied unit and manufacturer documentation.
- Product
- Ulthera System (Ultherapy)
- Manufacturer / brand
- Ulthera
- Equipment type
- Focused Ultrasound Aesthetic System
- Brand
- Merz
- Model / identifier
- era
- Device
- era
- Type
- Lasers
What to verify before ordering Ulthera
Use this checklist to avoid configuration or compatibility mismatches.
- Exact console/probe model and part number
- Software/revision and compatible transducers
- Licensed applications and DICOM/network options
- Probe/cable/connector/image-quality condition
- Battery/cart/display condition where applicable
- Service history and destination requirements
Ulthera manufacturer and regulatory resources
Use authoritative documentation to confirm model identity, compatibility, operating requirements and configuration-sensitive details.
FDA regulatory document
Technical or regulatory resource relevant to Ulthera product evaluation.
Ulthera technical resource
Technical or regulatory resource relevant to Ulthera product evaluation.
Frequently asked questions
Key questions for evaluating Ulthera before purchase.
What is Ulthera?
Ulthera is a focused ultrasound aesthetic system from Ulthera. FDA K121700 identifies the Ulthera System as an aesthetic focused-ultrasound device platform.
What should be checked before ordering Ulthera?
Exact console/probe model and part number; Software/revision and compatible transducers; Licensed applications and DICOM/network options.
Are all Ulthera configurations identical?
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.
What is included with Ulthera?
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.
Can Ulthera be shipped internationally?
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.
Ulthera documentation for Ulthera
Manufacturer names and trademarks are used for product identification. Confirm model-specific instructions, compatibility and regional requirements before use.
Procurement support for Ulthera
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.
Request a Ulthera quote
Include delivery country, quantity, required configuration and target purchase date for a destination-specific offer.
