Ansell, Inc.
Ansell, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1999.
Top product codes for Ansell, Inc.
Recent clearances by Ansell, Inc.
- K984392 — ANSELL CONDOMS
- K983518 — LIFESTYLES XTRA PLEASURE
- K940047 — SPERMICIDALLY LUBRICATED CONDOM
- K953379 — HYPOALLERGENIC POWDERED AMBIDEXTROUS COAGULATN DIPPED LATEX EXAMINATION GLOVE
- K945766 — HYPOALLERGENIC POWDERED AMBIDEXTROUS PATIENT EXAMINATION GLOVES
- K945767 — POWDER FREE, HYPOALLERGENIC AMBIDEXTROUS PATIENT EXAMINATION GLOVES
- K940045 — CONDOM
- K940046 — NON-LUBRICATED CONDOM
- K913766 — ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES
- K914760 — LATEX EXAMINATION GLOVES
- K903107 — PATIENT EXAM GLOVES (DUSTED W/USP STARCH POWDER)
- K903108 — PATIENT EXAM GLOVES (FINISH W/USP STARCH POWDER)
- K901111 — NUDA (CURRENTLY CALLED ULTRA SENSITIVE)
- K901112 — G.S.A. COLORED CONDOMS
- K897081 — ANSELL CONFORM GREEN EXAMINATION GLOVES
- K895660 — ANSELL DENTA GLOVES
- K892289 — PATIENT EXAMINATION GLOVES (LATEX)
- K892288 — PATIENT EXAMINATION GLOVES (LATEX)
- K892106 — STERILE EXAM GLOVES
- K892325 — NON-STERILE EXAM GLOVES
- K882389 — KISS OF MINT(TM) NON-LUBRICATED CONDOM
- K871304 — LIFESTYLES EXTRA STRENGTH CONDOMS W/NONOXYNOL-9
- K864400 — EXTRA STRONG CONDOM
- K850635 — ANSELL NO POWDER SURGEON'S GLOVES
- K831565 — MICRO-THIN SURGICAL GLOVE
- K831564 — ORTHOPEDIC SURGICAL GLOVE
- K830691 — PRIME
- K822792 — NUDA-PLUS CONDOM W/SPERMICIDAL LUBRICANT
- K820665 — DERMA PRENE
- K802641 — GAMMEX SURGICAL GLOVES
Data sourced from openFDA. This site is unofficial and independent of the FDA.