Company · US
Medipurpose Pte. , Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2022. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Sep 22, 2022 | K222224 | SurgiLance® Safety Lancet Medipurpose Pte. , Ltd., SG | FMK |
| Feb 11, 2013 | K130132 | BABYLANCE HEEL INCISION DEVICE Medipurpose Pte. , Ltd. | FMK |
| Sep 1, 2011 | K110062 | MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG Medipurpose Pte. , Ltd. | FRO |
| Oct 21, 2010 | K101145 | SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250 Medipurpose Pte. , Ltd. | FMK |
| Oct 19, 2010 | K101417 | BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200 Medipurpose Pte. , Ltd. | FMK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||