Merz North America, Inc.
4 FDA 510(k) clearances · Recalling firm
◉ Watch Merz North America, Inc.
| Record | Firm | Date |
|---|---|---|
| Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. recall (Z-2607-2016) | Merz North America, Inc. | 2016-08-19 |
| Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal im recall (Z-0366-2016) | Merz North America, Inc. | 2015-12-03 |
| PROLARYN Injectable Implant 1.0 cc Gel, Model No. 8602M0K5. A restorable implant material recall (Z-0367-2016) | Merz North America, Inc. | 2015-12-03 |
| PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA) Injectable Imp recall (Z-0368-2016) | Merz North America, Inc. | 2015-12-03 |
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Every clearance here is in the API, with alerts when new ones post.