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 Boston ScientificLabelled by claude-sonnet-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 Bridgepoint Medical with 14 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Nov 8, 2012: STINGRAY GUIDEWIRES.
| Nov 8, 2012 | STINGRAY GUIDEWIRESK122795 · DQX | 510(k) clearances |
| Jul 13, 2012 | MANTARAY GUIDEWIRESK121745 · DQX | 510(k) clearances |
| Jun 26, 2012 | BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only, Manufacturer BridgePoint MedicClass II · BridgePoint Medical Inc. is voluntarily recalling Stingray Catheter, Model M1000 lots BP20121440078 and BP20121560089. | Device recalls |
| May 22, 2012 | BIGBOSS CATHETERS MANTATAY CATHETER MANTARAY GUIDEWIRESK120533 · PDU | 510(k) clearances |
| Apr 18, 2012 | MANTARAY GUIDEWIRESK120881 · DQX | 510(k) clearances |
| Feb 3, 2012 | MANTARAY CATHETERK120129 · DQY | 510(k) clearances |
| Jan 4, 2012 | BIGBOSS CATHETERK113589 · DQY | 510(k) clearances |
| Aug 10, 2011 | BRIDGEPOINT MEDICAL MANTARAY(TM) CATHETERK111963 · DQY | 510(k) clearances |
| Jun 30, 2011 | MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003K111488 · DQX | 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
