Company ยท US
Ansell, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1999. Name variants (Inc, Corp, punctuation) are merged.
30510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 21, 1999 | K984392 | ANSELL CONDOMS Ansell, Inc. | HIS |
| Jul 6, 1999 | K983518 | LIFESTYLES XTRA PLEASURE Ansell, Inc. | HIS |
| Dec 19, 1995 | K940047 | SPERMICIDALLY LUBRICATED CONDOM Ansell, Inc. | HIS |
| Sep 27, 1995 | K953379 | HYPOALLERGENIC POWDERED AMBIDEXTROUS COAGULATN DIPPED LATEX EXAMINATION GLOVE Ansell, Inc. | LYY |
| Aug 7, 1995 | K945766 | HYPOALLERGENIC POWDERED AMBIDEXTROUS PATIENT EXAMINATION GLOVES Ansell, Inc. | LYY |
| Mar 2, 1995 | K945767 | POWDER FREE, HYPOALLERGENIC AMBIDEXTROUS PATIENT EXAMINATION GLOVES Ansell, Inc. | LYY |
| Jan 30, 1995 | K940046 | NON-LUBRICATED CONDOM Ansell, Inc. | HIS |
| Jan 30, 1995 | K940045 | CONDOM Ansell, Inc. | HIS |
| Mar 11, 1993 | K913766 | ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES Ansell, Inc., TH | LYY |
| Jan 17, 1992 | K914760 | LATEX EXAMINATION GLOVES Ansell, Inc. | LYY |
| Aug 29, 1990 | K903108 | PATIENT EXAM GLOVES (FINISH W/USP STARCH POWDER) Ansell, Inc., TH | LYY |
| Aug 29, 1990 | K903107 | PATIENT EXAM GLOVES (DUSTED W/USP STARCH POWDER) Ansell, Inc., TH | LYY |
| Mar 27, 1990 | K901112 | G.S.A. COLORED CONDOMS Ansell, Inc. | HIS |
| Mar 27, 1990 | K901111 | NUDA (CURRENTLY CALLED ULTRA SENSITIVE) Ansell, Inc. | HIS |
| Mar 26, 1990 | K897081 | ANSELL CONFORM GREEN EXAMINATION GLOVES Ansell, Inc., TH | LYZ |
| Jan 2, 1990 | K895660 | ANSELL DENTA GLOVES Ansell, Inc., TH | LYY |
| Jun 23, 1989 | K892289 | PATIENT EXAMINATION GLOVES (LATEX) Ansell, Inc. | LYY |
| Jun 9, 1989 | K892288 | PATIENT EXAMINATION GLOVES (LATEX) Ansell, Inc. | LYY |
| May 31, 1989 | K892325 | NON-STERILE EXAM GLOVES Ansell, Inc. | LYY |
| May 31, 1989 | K892106 | STERILE EXAM GLOVES Ansell, Inc. | LYY |
| Oct 20, 1988 | K882389 | KISS OF MINT(TM) NON-LUBRICATED CONDOM Ansell, Inc. | HIS |
| Jun 11, 1987 | K871304 | LIFESTYLES EXTRA STRENGTH CONDOMS W/NONOXYNOL-9 Ansell, Inc. | HIS |
| Feb 2, 1987 | K864400 | EXTRA STRONG CONDOM Ansell, Inc. | HIS |
| Jun 26, 1985 | K850635 | ANSELL NO POWDER SURGEON'S GLOVES Ansell, Inc. | KGO |
| Jul 19, 1983 | K831565 | MICRO-THIN SURGICAL GLOVE Ansell, Inc. | KGO |
| Jul 12, 1983 | K831564 | ORTHOPEDIC SURGICAL GLOVE Ansell, Inc. | FMC |
| Mar 31, 1983 | K830691 | PRIME Ansell, Inc. | HIS |
| Sep 30, 1982 | K822792 | NUDA-PLUS CONDOM W/SPERMICIDAL LUBRICANT Ansell, Inc. | HIS |
| May 3, 1982 | K820665 | DERMA PRENE Ansell, Inc. | KGO |
| Dec 11, 1980 | K802641 | GAMMEX SURGICAL GLOVES Ansell, Inc. | KGO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||