Surgical Robots Parts

Surgical Robots Parts
Details:
Surgical robots parts refer to manufacturing precision components for medical robotic systems through CNC machining, grinding, and micro-finishing. Strongd serves Class I/II medical device manufacturers, producing instrument joints, forceps shafts, camera arms, motor housings, and sterile adapters. From prototyping to FDA-compliant production, we deliver traceable, biocompatible solutions.
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Description
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1

Surgical robots parts refer to manufacturing precision components for medical robotic systems through CNC machining, grinding, and micro-finishing. Strongd serves Class I/II medical device manufacturers, producing instrument joints, forceps shafts, camera arms, motor housings, and sterile adapters. From prototyping to FDA-compliant production, we deliver traceable, biocompatible solutions.

Advantages

Medical-Grade Precision

Tolerances: ±0.005mm for instrument articulation

Surface finish: Ra ≤0.1μm (mirror polish for reduced tissue drag)

Biocompatibility: ISO 10993-5 certified materials

Sterilization Resilience

Withstands 1,000+ cycles of:

Autoclaving (134°C steam)

EtO gas

Hydrogen peroxide plasma

Zero corrosion: Passivated per ASTM A967

Regulatory Compliance

Full material traceability (UDI-compliant)

FDA 21 CFR Part 820 / ISO 13485 processes

Cleanroom assembly (ISO Class 7)

Applications

Prototyping validates kinematics and sterilization integrity. Critical components include:

Articulated instruments: Wrist joints, needle drivers

Imaging systems: Endoscope couplers, lens mounts

Robotic arms: Carbon fiber-reinforced segments

Sterile barriers: Polymer adapters with hermetic seals

Surface Treatment

Electropolishing: Ra 0.05μm (ultra-smooth bearing surfaces)

PVD Coatings: CrN/TiAlN for wear resistance (≥500k cycles)

Laser marking: UDI codes & lot numbers

Anodizing (titanium): Color-coding for instrument ID

Why Choose Strongd?

 

Our ISO 13485:2016-certified facility features medical-dedicated CNC cells with integrated metrology. Engineers with 10+ years of surgical device expertise provide DFM guidance, validate cleanroom protocols, and deliver full DHRs (Device History Records). 100% of clients pass FDA audits with our parts.

Production Process

 

 
 

Design Review

Analyze CAD models (SolidWorks/STEP)

Risk assessment per ISO 14971

 
 

Material Certification

Medical-grade metals: 316LVM, Ti-6Al-4V ELI

USP Class VI plastics: PEEK, PEI, PPSU

Mill certs + biocompatibility reports

 
 

Precision Machining

Swiss turning (Ø0.1–32mm shafts)

5-axis micro-milling (±0.005mm)

 
 

Deburring

Cryogenic deflashing for micro-features

Ultrasonic cleaning (DI water/medical ethanol)

 
 

Surface Enhancement

Electropolishing/Passivation

Medical PVD coating

 
 

Inspection

Vision systems: 5μm feature measurement

CMM with GD&T reporting (ASME Y14.5)

 
 

Cleanroom Assembly

Press-fit bearings, laser welding

Particulate monitoring

 
 

Sterile Packaging

Double-barrier Tyvek pouches

Gamma irradiation validation

FAQ

 

Q1: How fast for prototype delivery?

A1: 10–15 days (including surface treatments).

Q2: Can you supply RoHS/REACH-compliant materials?

A2: Yes – full material declarations provided.

Q3: Do you validate sterilization cycles?

A3: Yes – we partner with ISO 17025 labs for validation reports.

Q4: Minimum feature size?

A4: 0.15mm micro-channels, Ø0.2mm holes.

Q5: Batch traceability?

A5: Laser-marked UDI + electronic DHR per lot.

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