Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medical Device Services with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 14, 2002: REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS.
| Nov 14, 2002 | REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPSK022753 · JOW | 510(k) clearances |
| Nov 4, 2002 | REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPSK022751 · KGE | 510(k) clearances |
| Oct 9, 2002 | REPROCESSED DISPOSABLE TROCARSK022743 · KAB | 510(k) clearances |
| Oct 9, 2002 | REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERSK022748 · HET | 510(k) clearances |
| Sep 18, 2002 | REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSK022744 · HWE | 510(k) clearances |
| May 8, 2002 | COMPRESSIBLE LIMB SLEEVEK012979 · JOW | 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
