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 15, 2026, FDA's public records list Nobelpharma USA, Inc. with 64 510(k) clearances. The most recent is a 510(k) clearance dated Jun 28, 1999: BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USE.
| Jun 28, 1999 | BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USEK984162 · MAH | 510(k) clearances |
| Sep 6, 1996 | NOBLEPHARMA WIDE ACCESSORIESK962403 · DZE | 510(k) clearances |
| Aug 9, 1996 | NOBELPHARMA BONE ANCHORED HEARING AIDK955713 · LXB | 510(k) clearances |
| Jul 22, 1996 | BRANEMARK SYSTEMS MKII SELK-TAPPING FIXTUREK962130 · DZE | 510(k) clearances |
| Jul 18, 1996 | 17 ANGULATED ABUTMENTK961736 · NHA | 510(k) clearances |
| Jul 10, 1996 | CERA ONE ABUTMENT SYSTEMK961737 · DZE | 510(k) clearances |
| Jul 10, 1996 | MIRUSCONE ABUTMENT SYSTEMK961728 · NHA | 510(k) clearances |
| May 14, 1996 | ABUTMENT SELECTION KITK960639 · DZE | 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
