Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Asia-Med GmbH and Co KG and its 1 subsidiaries with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 2, 2013: CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE:….
| Dec 2, 2013 | CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE: METAL HANDLE WITHOUT GUIDE TUBEK132896 · MQX | 510(k) clearances |
| Oct 14, 2005 | STANDARD, SPECIAL, SPECIAL+, SNEEDLE B-TYPE AND SNEEDLE J-TYPE ACUPUNCTURE NEEDLESK052085 · MQX | 510(k) clearances |
| Oct 14, 2004 | PRESS TACK NEEDLEK042063 · MQX | 510(k) clearances |
| Jul 10, 2003 | SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPEK031716 · MQX | 510(k) clearances |
| Jul 10, 2001 | ASIA-MED ACUPUNCTURE NEEDLES, (STANDARD, SPECIAL, COMPACT, APEX)K011808 · MQX | 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
