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 Arthropedics, Inc. with 29 510(k) clearances. The most recent is a 510(k) clearance dated Jan 14, 1988: ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS).
| Jan 14, 1988 | ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)K873619 · HRX | 510(k) clearances |
| Dec 15, 1987 | MONOPOLAR CAUTERY BLADE TIP #TM-1701K873653 · JOS | 510(k) clearances |
| Dec 15, 1987 | MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873654 · JOS | 510(k) clearances |
| Dec 15, 1987 | MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873655 · JOS | 510(k) clearances |
| Nov 25, 1987 | VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873387 · HXR | 510(k) clearances |
| Nov 2, 1987 | SERRATED GRASPING FORCEPS, CURVED UPK873513 · HTD | 510(k) clearances |
| Nov 2, 1987 | MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350K873710 · HWB | 510(k) clearances |
| Nov 2, 1987 | CUP BIOPSY FORCEPS, CURVED DOWNK873505 · HTD | 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
