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 15, 2026, FDA's public records list Instrument Makar with 28 510(k) clearances. The most recent is a 510(k) clearance dated Nov 15, 2000: LITWIN CRUICATE ANCHOR.
| Nov 15, 2000 | LITWIN CRUICATE ANCHORK002600 · MBI | 510(k) clearances |
| Nov 6, 1998 | ST LEGER CEMENTED SEMI-CONSTRAINED TOTAL KNEE IMPLANTK980999 · JWH | 510(k) clearances |
| May 6, 1997 | BIOSPHERE SUTURE ANCHORK963396 · MAI | 510(k) clearances |
| Feb 25, 1997 | DISPOSABLE APRONK964364 · LYU | 510(k) clearances |
| Nov 19, 1996 | FLUID BARRIER BOOT KNEE & ANKLE-HIGHK955835 · FXP | 510(k) clearances |
| Jul 9, 1996 | BIOASBSORBABLE MINI-SCREW SUTURE ANCHORK960555 · MAI | 510(k) clearances |
| Jul 31, 1995 | BIOABSORBABLE INTERFERENCE SCREWK943249 · MAI | 510(k) clearances |
| Feb 23, 1995 | LAPRASCOPIC GRASPERK944062 · GCS | 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
