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., part of Zimmer Biomet HoldingsLabelled 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 Arthrotek with 17 510(k) clearances. The most recent is a 510(k) clearance dated Sep 25, 2006: ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE.
| Sep 25, 2006 | ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICEK061776 · JDR | 510(k) clearances |
| Aug 7, 2006 | 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORSK061801 · JDR | 510(k) clearances |
| Jul 25, 2006 | HITCH LACTOSORB SUTURE ANCHORK061657 · JDR | 510(k) clearances |
| Jul 19, 2006 | ALLTHREAD LACTOSORB SUTURE ANCHORK061389 · JDR | 510(k) clearances |
| Jun 6, 2006 | MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHORK060693 · HWC | 510(k) clearances |
| Feb 3, 2006 | EZLOC FEMORAL FIXATION DEVICEK053461 · MBI | 510(k) clearances |
| Jun 29, 2005 | NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHERK051069 · MBI | 510(k) clearances |
| Oct 29, 2004 | TI - SCREW ANCHOR SPK042460 · MBI | 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
