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For regulated medical manufacturing teams

AI visual inspection with traceable, replayable evidence for every unit.

Controlled inspection that proves coverage and seals tamper-evident evidence — built for environments where every decision must be defensible.

Run the live inspection cycleBuild a station fit report

Regulated Medical Device inspection-to-evidence story

  1. Step 1: the Regulated Medical Device inspection cell is running.
  2. Step 2: inspection identifies surface defect on a critical feature.
  3. Step 3: sealed evidence: coverage · rule version · model version.
  4. Step 4: a NCR draft is prepared — ncr draft prepared, linked to the risk file.
  5. Step 5: human approval is required before any decision; nothing is released or closed automatically.
  6. Step 6: audit packet ready for the released unit.

From factory signal to audit-ready record

Human-controlled
System preparedHuman approval requiredNo automatic release

Where teams usually start

  1. Final visual inspection
  2. Assembly / feature verification
  3. Molded-part verification

Example part & rule

Example part Machined titanium implant body

Reject a surface pit above 0.2 mm in a critical region.

measured 0.35 mmlimit 0.2 mm
REJECT
surface pitscratchcontaminationmolding flaw

Discovery questions for the conversation

Which inspection station should we map first?

The goal is to identify one station where this could matter — then validate with your approved parts and criteria.

Build the deployment plan

This is an example workflow for regulated medical deviceteams — a hypothesis, not a claim about any specific company's process.

Demo scenes are illustrative and use deterministic product scenarios. Regulated decisions remain human-controlled.