Medical High Technology International, Inc. FDA Record
Medical High Technology International, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Medical High Technology International, Inc." is on file.
- Latest 510(k)
- Nov 2, 1987
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 1 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Reviewing Medical High Technology International, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check Medical High Technology International, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K873580 | MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR | Nov 2, 1987 |
Medical High Technology International, Inc. and the FDA: common questions
Has Medical High Technology International, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Medical High Technology International, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Medical High Technology International, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Medical High Technology International, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
Need more than this page shows? Ask about Medical High Technology International, Inc. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.