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.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Regeneration Technologies, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 2008: REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSE….
| Apr 30, 2008 | REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PASTK080418 · NUN | 510(k) clearances |
| Jan 25, 2008 | BIOSET XCHK072238 · MQV | 510(k) clearances |
| Oct 24, 2007 | CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTONK072327 · MQV | 510(k) clearances |
| May 9, 2007 | STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937K063584 · HWC | 510(k) clearances |
| Sep 6, 2006 | BIOSET XCK060180 · MBP | 510(k) clearances |
| Feb 23, 2006 | STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.K060253 · HWC | 510(k) clearances |
| Nov 16, 2005 | STERLING INTERFERENC SCREW HTK052405 · HWC | 510(k) clearances |
| Aug 15, 2005 | STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBESK051615 · MQV | 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
