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 Woodlyn, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Jun 25, 1993: WOODLYN OPERATION MICROSCOPE.
| Jun 25, 1993 | WOODLYN OPERATION MICROSCOPEK931303 · FSO | 510(k) clearances |
| Jul 30, 1992 | WOODLYN CLASSIC LENSMETERK920861 · HLM | 510(k) clearances |
| Feb 21, 1990 | WOODLYN SLIT LAMP MODEL HR-1K900476 · HJO | 510(k) clearances |
| Feb 21, 1990 | WOODLYN FULL APERTURE TRIAL LENS SETK900478 · HPC | 510(k) clearances |
| Feb 21, 1990 | WOODLYN CLASSIC SLIT LAMP MODEL SMMK900477 · HJO | 510(k) clearances |
| May 17, 1989 | WOODLYN OPHTHALMIC PROJECTORK890992 · HOS | 510(k) clearances |
| Dec 23, 1987 | WOODLYN CLASSIC REFRACTOR, PHOROPTORK874900 · HKN | 510(k) clearances |
| Dec 11, 1984 | WOODLYN CLASSIC CATARACT ACUITY TESTK843812 · HLI | 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
