
Grade 2 Titanium
Standard: UNS R50400 · ASTM B348 applicable scope
Solid · Hollow · Hemispheres · Float
Source titanium balls, spheres, hemispheres and float balls with grade, diameter, tolerance, surface, finish and inspection reviewed against your order requirements.
Buying Essentials
Grade, UNS, specification and revision, condition and supplementary requirements.
Diameter, section, length, quantity, tolerance and machining allowance.
Tolerance, surface, finish, end condition and acceptance criteria.
MTC, traceability, inspection, testing, marking, packing and release documents.
Grade Reference
Titanium Balls & Spheres grades and product forms reviewed against ASTM / ASME / project specifications.

Standard: UNS R50400 · ASTM B348 applicable scope

Standard: UNS R56400 · ASTM B348 / AMS 4928

Standard: UNS R52400 · ASTM B348

Standard: UNS R56407 · ASTM B348 / F136
Process Review
Each step closes one part of the order basis. Titanium Balls & Spheres preparation, processing and inspection scope are confirmed by quotation against the approved order basis.

Grade, specification, condition, dimensions, quantity and document scope aligned before supply.

Source form, condition, identity and applicable specification confirmed against the quotation.

Cut route, allowance, edge condition and surface requirements controlled to the agreed scope.

Order-specific dimensional, surface, material or third-party checks completed as agreed.

Identification, document set, protective packing and delivery basis checked before release.
Inside Titanium Parts
Titanium Balls & Spheres preparation, processing and inspection are carried out in our own facility. The inspection scope and documentation for a specific order are agreed in the quotation.
Application Context
Grade, condition and documentation choices follow from the operating environment, not from the section name. Each context below sets the typical qualification conversation before the first quotation.

Confirm ball geometry, mating parts, sealing, pressure class and assembly-level validation.

State load, lubrication, clearance, surface and assembly-level performance testing scope.

Confirm wall, density, leak test, weld procedure and assembly boundary.

Separate ASTM F67 / F136 conformity from finished-device approval, clinical suitability and sterilization validation.
Supply Scope & Qualification
A certificate name alone does not define the complete acceptance package. State the traceability level, inspection characteristics, test reports, marking, third-party involvement and release documents required by the order.
Grade, specification revision, condition and heat or lot reference.
Measured characteristics, method, sampling, tolerance and report format.
Mechanical, NDT or third-party checks stated in the agreed scope.
Required certificate index, language, approval route and delivery timing.
Before You Order
Four checks that catch most order-basis errors before they become commercial or quality problems.
Grade, form, specification revision, condition and heat or lot basis.
Size, tolerance, surface, allowance, processing route and responsibility.
Certificates, measurements, tests, hold points and acceptance criteria.
Quantity basis, exclusions, packing, Incoterm and schedule assumptions.
Questions
Common questions before sending the inquiry.
Provide the grade, governing specification and revision, condition, dimensions, quantity, surface, processing, inspection, testing and document requirements. A drawing is optional for the first enquiry and especially useful for non-standard or drawing-based items.
Common enquiries include Grades 2, 5, 7 and 23. Other grades may be reviewed. Availability, source form, condition, size and applicable specification are confirmed for the specific quotation.
Yes, drawing-based items can be reviewed against the required geometry, grade, condition, tolerance, machining allowance, processing route and quantity. The accepted process and final scope are stated in the quotation.
No. Required certificates, traceability level, dimensional records, testing, NDT and third-party involvement should be specified before quotation. Only the agreed package is included in the order scope.
No. A raw-material specification does not establish finished-device approval, clinical suitability, sterilization validation, regulatory compliance or application qualification. Those responsibilities remain with the device or system manufacturer.
No. They depend on grade, source form, condition, size, tolerance, processing, inspection, quantity and documentation. Confirm the exact combination during quotation review.