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 Techhnilab Instruments, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 31, 1981: ELECTRIC SELF STERILIZATION INOCUL. LOOP.
| Date | Record | Source |
|---|---|---|
| Dec 31, 1981 | ELECTRIC SELF STERILIZATION INOCUL. LOOPK813523 · LTB | 510(k) clearances |
| May 26, 1978 | THERMAJUST CIRCU-TEMPK780543 · JRQ | 510(k) clearances |
| Apr 24, 1978 | DISC-PAK ROTATORK780544 · GLE | 510(k) clearances |
| Aug 22, 1977 | MULTI-CAVITY EQUILIBRIUM CELLK771434 · | 510(k) clearances |
| Jan 28, 1977 | MADDATHERM PARAFFIN BATHK770170 · IMC | 510(k) clearances |
| Jan 28, 1977 | BEESON AUTOMADDAK FEEDERK770169 · ILC | 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
