CoCrMo
CoCrMo powder supplier and RFQ
Wear- and corrosion-resistant cobalt alloy powder for dental, medical-development, and industrial wear parts.
- CoCrMo
- Cobalt chromium molybdenum
- PSD candidates
- 15–45 µm · 15–53 µm · 45–106 µm
- Process routes
- LPBF · EBM · MIM
- Commercial path
- Quote by specification
Final price, availability, lead time, chemistry, performance data, and documentation are confirmed for the quoted specification and lot.
Alloy identification
Specify this powder by grade, then narrow the buying requirement.
CoCrMo and cobalt-chromium-molybdenum cover multiple chemistry and program variants. State the governing standard, revision, and intended use instead of relying on the family name.
Similar grade names do not establish identical chemistry or process compatibility. Include the governing specification and required edition; the quotation confirms the proposed powder and supporting lot records.
Specification controls
Define the powder beyond the alloy designation.
The same grade name can represent materially different powder routes. A usable RFQ needs the acceptance method, limits, packaging, and intended process.
Chemistry & standard
State the governing grade, revision, restricted elements, and any tighter oxygen or nitrogen limits.
PSD & method
Choose a candidate range and state whether sieve, laser diffraction, or a customer method controls acceptance.
Powder behavior
Define required flow, apparent/tap density, morphology evidence, satellites, and hollow-particle limits where relevant.
Lot & reuse plan
Confirm lot size, virgin/reused powder policy, blend restrictions, sampling, retention, and traceability expectations.
Process and PSD
Process and PSD options to confirm in the RFQ.
PSD labels below are catalog starting points. Final fit depends on the machine, layer strategy, feed system, qualification plan, and the supplier lot.
| Decision variable | Catalog starting points | Required confirmation |
|---|---|---|
| Process candidates | LPBF · EBM · MIM | Machine, feed system, layer strategy, and qualification stage |
| PSD candidates | 15–45 µm · 15–53 µm · 45–106 µm | Target process, equipment limits, and PSD test method |
| Process × PSD pairing | Not implied by this catalog page | Confirmed in the RFQ against the selected source and lot |
Powder screening data
A screening window for a better technical RFQ.
These grade-specific values help define the questions to ask. They are not stock data, a universal specification, or a lot certificate.
| Powder metric | Screening value | Qualification boundary |
|---|---|---|
| D10 | ≥12 µm | Method and lot to be confirmed |
| D50 | 25–40 µm | Method and lot to be confirmed |
| D90 | ≤65 µm | Method and lot to be confirmed |
| Sphericity | ≥0.85 | Method to be confirmed |
| Apparent density | ≥4.4 g/cm³ | Method and lot to be confirmed |
| Tap density | ≥5.0 g/cm³ | Method and lot to be confirmed |
| Flow | ≤25 s/50 g | Method and conditioning to be confirmed |
LPBF / EBM screening window. A CoCrMo screening basis; the exact chemistry version and medical or dental release scope must be confirmed. Ask for the governing test method, sampling rule, source, production route, and lot-linked report in the quotation.
Application fit
Applications suited to technical review.
Dental frameworks
Wear-critical hardware
Valve and pump wear components
Failure modes
Critical variables to verify before qualification.
- Exact chemistry version
- Biocompatibility responsibility
- Finished-part validation
Evidence package
Request the documents that support the actual buying decision.
State the exact chemistry or customer standard, intended dental, medical-development, or industrial use, and the responsible finished-part validation route.
Certificates, technical data, sample reports, and partner-specific documents are supplied only when they correspond to the quoted source, grade, particle-size route, and lot.
Price and supplier RFQ
Price and availability follow the exact grade, PSD, evidence, and delivery scope.
A useful supplier comparison keeps the technical and commercial basis identical. Send the same inputs to avoid comparing different chemistry limits, powder routes, packages, or document scopes as if they were the same product.
Grade and acceptance basis
State the exact chemistry or customer standard, intended dental, medical-development, or industrial use, and the responsible finished-part validation route.
Process, machine, and PSD
State the target process, equipment constraints, particle-size range, and governing PSD method.
Quantity, packaging, and destination
Separate sample and production quantities; include package size, destination country, and target timing.
Lot evidence and source controls
List required COA, PSD, SDS, TDS, SEM, traceability, sampling, and production-route evidence.
Custom chemistry or PSD?