Implant-grade verification • Lot traceable • Professional manufacturing

Grade 23 Titanium Verified to ASTM F136

Implant-grade titanium alloy (Ti-6Al-4V ELI / Grade 23) with complete documentation, lot traceability, and an ISO 9001 quality management system. Built for professional piercing applications where consistency and safety matter.

Traceability
Heat/Lot → Batch → Shipment
Delivery
PDF, signed/stamped on request
NDA
Available for compliance files

Material & Verification

Alloy / Grade Ti-6Al-4V ELI (Grade 23)
Specification ASTM F136 verification
Biocompatibility Test methods per ISO 10993 (on request)
100%
Lot Traceable
CoC
Each Shipment
Included by default
  • CoC (Certificate of Conformance/Compliance)
  • MTC / Mill Test Certificates (where applicable)
  • Batch/lot traceability statement

Material Excellence

We focus on titanium manufacturing to support batch consistency, stable finishing, and reliable documentation for professional piercing supply chains.

Why Titanium Focus?

Biocompatibility-first

Grade 23 titanium alloy verified to ASTM F136 requirements for implant-grade expectations in high-sensitivity applications.

Batch-to-batch consistency

Standardized processes, dedicated tooling, and documented parameters reduce variability across production lots.

Traceability you can audit

Lot/heat references link raw material records to production batches and shipments for QA and regulatory needs.

Documentation-ready supply

CoC and supporting files can be prepared in PDF format; signed/stamped versions available upon request.

Specification vs Grade (Quick Reference)

Item
Grade 23
ASTM F136

What it is
Material grade (Ti-6Al-4V ELI)
Standard/specification for surgical implant alloy requirements
Focus
Alloy identity
Chemistry, mechanicals, and quality requirements per the standard
How we use it
Primary alloy we manufacture
Verification basis for implant-grade expectations
Note: Documentation availability and verification scope may vary by program and customer requirements. Request files for the exact lot/batch you need.

Documentation Checklist (Typical)

Material Files
  • Material statement (Grade 23 / ASTM F136 basis)
  • Mill test certificates (if applicable)
  • Chemistry / composition summary
Quality & Traceability
  • CoC for each shipment
  • Lot/heat → batch → shipment traceability
  • Inspection / dimensional reports (as required)
Need a specific format (signed, stamped, or customer template)? Select “Additional Requirements” in the request form below.

Compliance & Certifications

Quality management and ethical audit programs support consistent manufacturing and responsible supply chain expectations.

ISO 9001

Quality Management System

ISO 9001 controls documentation, process consistency, and corrective/preventive action workflows across procurement, production, and final inspection.

Document control and process standardization
Risk-based thinking and preventive actions
Customer requirements review and monitoring
Continuous improvement and internal audits

SMETA

Ethical Trade Audit Program

SMETA audit coverage supports responsible manufacturing practices and supply-chain transparency expectations.

Labor standards and worker rights
Health and safety management
Environmental responsibility
Business ethics and anti-corruption

Available Documentation

A complete documentation package can be prepared for compliance review, QA validation, and customer onboarding.

Certificates

  • ISO 9001 Certificate
  • SMETA Audit Report
  • Business / Export Credentials (as applicable)
  • NDA template (optional)

Material Documentation

  • Material statement (Grade 23 / ASTM F136 basis)
  • Mill test certificates (if applicable)
  • Lot/heat reference summary
  • Chemical composition summary

Quality Records

  • Inspection reports (visual/dimensional as required)
  • QC records (process/finish controls)
  • Batch traceability statement
  • CoC (each shipment)

Frequently Asked Questions

Common questions about titanium grades, documentation, traceability, and quality assurance.

What’s the difference between Grade 23 and ASTM F136?

Grade 23 refers to the titanium alloy (Ti-6Al-4V ELI). ASTM F136 is a standard/specification that defines requirements for this alloy when used for surgical implant applications. In practice, we manufacture with Grade 23 alloy and verify documentation and requirements against ASTM F136 expectations when requested.

If you need a specific customer template or third-party verification scope, include it in the request form.

Do you support lot traceability and third-party testing?
  • Lot Traceability: Heat/lot references link raw material records to production batches and shipment documentation.
  • Third-Party Testing: We can provide samples for independent lab verification (composition, surface, or other tests), based on your required standard and scope.
  • Documentation: CoC, traceability statements, and inspection records can be prepared per program requirements.
How do you ensure consistent quality across batches?
  • Standardized processes: ISO 9001 procedures with controlled parameters and revision management.
  • Incoming qualification: Verification against required material documentation and specs per program.
  • In-process controls: Dimensional and finish checks defined in SOP and QC records.
  • Traceability: Lot linkage supports audit and rapid corrective action if needed.
What do you provide with each shipment?
  • CoC: Shipment-level certificate confirming conformance to the specified program requirements.
  • Traceability statement: Heat/lot → batch → shipment references (as applicable).
  • Inspection records: Dimensional/visual reports based on agreed QC plan.
  • Supporting material files: Material statements and mill certificates when included in your program.
Can you provide samples for verification?
  • Finished samples: Pieces from the same processing route for lab verification.
  • Documentation support: Samples can be paired with the relevant lot/batch references.
  • Lab coordination: We can align on your chosen accredited lab and required test scope.

Request Documentation

Receive the documentation package you need for QA review, supplier onboarding, or compliance checks.

Required Documents (select at least one) *

Tip: If you need signed/stamped files or a specific customer template, note it below.

Response Window
4–8 Business Hours
Secure Handling
NDA Available

Documentation is provided under confidentiality terms when required. Your information is used only to respond to this request.