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 Exmoor Plastics with 43 510(k) clearances. The most recent is a 510(k) clearance dated May 10, 2010: EPIDRUM.
| May 10, 2010 | EPIDRUMK093863 · FMF | 510(k) clearances |
| Mar 5, 1999 | EXMOOR SUCTION CLEARANCE KITK990366 · LRC | 510(k) clearances |
| Oct 22, 1998 | EXMOOR MYRINGOTOMY KITK980828 · ETD | 510(k) clearances |
| Sep 14, 1998 | DILKES LASER/SUCTION CANNULAEK981143 · GEX | 510(k) clearances |
| Jul 16, 1998 | EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)K972700 · KHJ | 510(k) clearances |
| Jun 5, 1998 | MILLS COLUMELLA PROSTHESISK981088 · ETA | 510(k) clearances |
| May 20, 1998 | EXMOOR TEFLON LOOP REPLACEMENT PROSTHESISK981045 · ETB | 510(k) clearances |
| May 13, 1998 | PFLEIDERER'S INTRATYMPANIC CATHETERK974008 · ETD | 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
