Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 15, 2026, FDA's public records list Moyco Industries and its 1 subsidiaries with 20 510(k) clearances. The most recent is a 510(k) clearance dated Oct 11, 1996: CYBER-FIL ALKENOATE CEMENT MULTI-PURPOSE KIT (23900/23905/23910/23915/23920).
| Oct 11, 1996 | CYBER-FIL ALKENOATE CEMENT MULTI-PURPOSE KIT (23900/23905/23910/23915/23920)K962733 · EMA | 510(k) clearances |
| Apr 27, 1995 | MOYCO-EDTAK950365 · KJJ | 510(k) clearances |
| May 18, 1994 | RETRO MIRRORK941574 · EAX | 510(k) clearances |
| Mar 7, 1994 | THERMAL PULP TESTERK940260 · EAT | 510(k) clearances |
| Jan 3, 1994 | NICKEL-TITANIUM K-TYPE FILEK935542 · EKS | 510(k) clearances |
| Nov 5, 1993 | SILICONE MIRRORK932511 · EKJ | 510(k) clearances |
| May 27, 1993 | INJECT-R FILLK931742 · EKM | 510(k) clearances |
| Oct 20, 1992 | QUADRASORB FILTERK923661 · CAH | 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
