Zhejiang Kingstone Robot & Technology Co., Ltd.
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Closed Loop Robotic Grinding Polishing Machine For Medical Implant Components

Closed Loop Robotic Grinding Polishing Machine For Medical Implant Components
Place of Origin:CHINA
Brand Name:KINGSTONE
Certification:CE
Model Number:KS-CNC2
Minimum Order Quantity:1
Price:65000-98000 USD
Standard Packaging:WOODEN CASES
Delivery Time:90 WORKING DAYS
Payment Terms:L/C,D/A,D/P,T/T
Supply Ability:200-300 SETS PER YEAR
Product Details
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Closed Loop Grinding And Polishing Machine

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Polishing Machine for Medical Implant Components

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Closed Loop Robotic Grinding Polishing Machine

Dimensions: Approx. 2500mm X 2000mm X 1800mm
Automation Level: Fully Automated
Material Compatibility: Steel, Aluminum, Stainless Steel, Titanium, Composites
Control System: PLC With Touchscreen Interface
Workpiece Size Range: Up To 1000mm X 1000mm
Type: Automated Surface Finishing Equipment
Cycle Time: Adjustable, Typically 1-5 Minutes Per Piece
Weight: Approximately 1500 Kg
Robot Type: 6-axis Articulated Robot
Maximum Workpiece Weight: Up To 100 Kg
Power Supply: 220V/380V, 50/60Hz
Grinding/Polishing Tools: Interchangeable Abrasive Pads And Wheels
Application: Grinding And Polishing Of Metal And Non-metal Surfaces
Safety Features: Emergency Stop, Safety Guards, Light Curtains
Product Description
Detailed Specifications & Features
Closed-Loop Robotic Grinding And Polishing Machine For Medical Implant Components
Medical implant surface finishing is not a cosmetic operation. The Ra value on a tibial tray, a femoral stem or a dental abutment is a functional specification with direct biological consequences: too rough on the articulating face and wear debris accumulates in the joint; too smooth on the osseointegration surface and bone cells cannot anchor. Get the wrong Ra on the wrong surface of the same implant, and the device fails the patient — long after it has passed visual inspection.
The LR-GP-MED is a closed-loop robotic grinding and polishing machine built for the precision and compliance requirements of medical implant manufacturing. Closed-loop means the machine does not estimate Ra — it measures Ra on every part, on every critical surface, and adjusts the process in real time until the specification is met. Every part exits the cell with a documented, traceable Ra record tied to its serial number, ready for your ISO 13485 Device History Record.
For implant manufacturers who cannot afford a surface-related field failure, this is the finishing cell that closes the gap between dimensional machining and biological performance.
LR-GP-MED Closed-Loop Robotic Grinding and Polishing Machine for medical implant components
Closed-Loop Process Overview
Two in-line Ra measurements gate the process. The first (post-G2) confirms the grinding handoff Ra before polishing begins — if grinding didn't achieve the target, a correction pass runs before the part moves to the polishing wheel. The second (post-P2) confirms the final Ra against the biocompatibility specification. If the measured Ra is within the target band, the part exits with a pass record. If not, one correction pass runs and Ra is re-measured. If still non-conforming after correction, the part is flagged — it does not leave the cell as conforming. The Ra record (both measurements, programme version, correction pass count) is written to the DHR data record before the part exits. No implant leaves the cell with an assumed Ra.

Key Proprietary Features
Dual In-Line Ra Measurement
Most finishing cells measure Ra offline, on a sample basis, after a batch is complete. The LR-GP-MED measures every part, in-line, at two process gates:
  • Gate 1 (post-G2): confirms grinding achieved the handoff Ra required for polishing to reach the final specification. If grinding Ra is too high, polishing cannot compensate — catching it here prevents polishing a part that will fail the final Ra gate.
  • Gate 2 (post-P2): confirms the finished part meets the biocompatibility Ra specification for its surface type (articulating vs osseointegration vs stem neck).
Heat-Damage-Free Titanium Finishing
Ti-6Al-4V develops a passive TiO₂ oxide layer that governs its biocompatibility. Grinding heat above [TBC]°C can alter the oxide stoichiometry — a change invisible to optical inspection but detectable by XPS surface analysis and potentially affecting osseointegration performance. The LR-GP-MED titanium protocol addresses this through three mechanisms:
  • Low-force, multi-pass grinding: force is set well below the threshold that generates frictional heat above [TBC]°C, using additional passes rather than single high-force cuts.
  • Surface temperature monitoring: an infrared sensor monitors the grinding zone surface temperature in real time; if temperature exceeds [TBC]°C, the cell pauses and flags the part.
  • Biocompatible coolant: a medical-grade coolant formulation (no mineral oil contaminants; [TBC] standard) is applied during grinding phases to manage heat at the contact zone.
CoCrMo Hard-Alloy Finishing
Cobalt-chrome-molybdenum alloy (ASTM F75 / F1537 [TBC]) resists abrasive finishing due to its high hardness (~35-45 HRC [TBC]) and carbide content. The risk in CoCrMo finishing is over-dwelling: the operator or open-loop machine applies extra dwell to achieve Ra, but extra dwell at one contact point creates directional scratch lines that become wear debris nucleation sites at the articulating interface. The LR-GP-MED CoCrMo recipe controls dwell per path point explicitly:
  • Maximum dwell per point: [TBC] s (recipe-capped)
  • If Ra at Gate 1 is not achieved within the dwell limit: the cell takes an additional pass (new path, new contact points) rather than extending dwell on existing points
  • Abrasive change frequency for CoCrMo is accelerated vs titanium — the wear counter is calibrated to the faster wheel degradation on hard alloy
Result: CoCrMo articulating surfaces are finished to Ra specification without directional scratch patterns. CoCrMo recipe dwell cap: [TBC] s; abrasive change interval: [TBC] cycles.

Frequently Asked Questions
What exactly does "closed-loop" mean for implant surface finishing?
It means the machine measures Ra in-line on every part at two process gates and uses those measurements to control the process — not to record it after the fact. Gate 1 (post-grinding) confirms the Ra handoff before polishing starts; if grinding didn't reach target, a correction pass runs before polishing begins. Gate 2 (post-polishing) confirms the final Ra against the biocompatibility specification; if it's out of window, one correction pass runs and Ra is re-measured. If still non-conforming, the part is flagged — it does not leave the cell as conforming. Both Ra values are written to the per-part DHR record. Closed-loop means the Ra measurement drives the process, not the other way around.
How does the cell protect the osseointegration surface while polishing the articulating face?
The fixture design exposes only the surface designated for each phase. The articulating face is exposed during polishing phases; the osseointegration zone is shielded by the fixture. In addition, the polishing path has a hard boundary set [TBC] mm from the osseointegration zone boundary — the wheel cannot reach it. The boundary is defined in the recipe per implant model and confirmed with your drawing before programming.
We run Ti-6Al-4V and CoCrMo in the same production shift. Is cross-contamination prevented?
Yes — through RFID-enforced segregation at three levels: tools (separate magazine positions, RFID-tagged; mismatch stops the cell), fixtures (RFID-tagged per alloy family; mismatch blocks the programme) and coolant (separate circuits per alloy family). The inter-alloy cleaning protocol is logged in the DHR record. Ti particles on a CoCrMo surface and CoCrMo particles on a Ti surface are both prevented by hardware enforcement, not operator discipline.
How does the cell avoid heat damage to the Ti-6Al-4V oxide layer?
Three mechanisms: (1) low-force, multi-pass grinding protocol — force is set below the frictional heat threshold for Ti, using additional passes rather than high-force single cuts; (2) in-process IR thermal monitoring — if the grinding zone surface temperature exceeds [TBC]°C, the cell pauses and flags the part; (3) biocompatible coolant applied during grinding phases to manage contact-zone heat. Parts that trigger the temperature threshold are held for surface chemistry review before returning to the process.
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