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 14, 2026, FDA's public records list Diemolding Corp. and its 1 subsidiaries with 55 510(k) clearances. The most recent is a 510(k) clearance dated Oct 10, 1996: THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTH….
| Oct 10, 1996 | THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORTK962749 · BWF | 510(k) clearances |
| Jul 25, 1996 | MEDSHIELD/AEROCHAMBERK961455 · CCQ | 510(k) clearances |
| Jul 25, 1990 | ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANSK902713 · CAC | 510(k) clearances |
| Jul 18, 1990 | CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITORK902114 · BSK | 510(k) clearances |
| Mar 15, 1990 | RESPIREX 2K900754 · BWF | 510(k) clearances |
| Jun 23, 1989 | BREATHING MOUTHPIECEK893791 · BYP | 510(k) clearances |
| Oct 7, 1988 | NON-REBREATHING TEE PIECE (NRTP)K883988 · CBP | 510(k) clearances |
| Jun 22, 1988 | MICROCIRRUS MEDICAL NEBULIZERK881935 · CAF | 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
