Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Lorvic Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 11, 1987: U. V. GERMICIDAL UNIT.
| Date | Record | Source |
|---|---|---|
| Sep 11, 1987 | U. V. GERMICIDAL UNITK871615 · KMH | 510(k) clearances |
| May 3, 1978 | SHIELDK780263 · EJK | 510(k) clearances |
| Jan 14, 1977 | FLUORIDE GEL DISPOSABLE TRAYK770064 · KMT | 510(k) clearances |
| Jan 14, 1977 | DISP. ABSORBENT COMPRESSED FIBRE WAFERK770063 · EFN | 510(k) clearances |
| Sep 21, 1976 | SALIVA EJECTORK760620 · DYN | 510(k) clearances |
| Jul 16, 1976 | IMPULSE HEAT SEALERK760121 · | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
