Carl Zeiss Suzhou Co., Ltd.
Carl Zeiss Suzhou Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2018, with 1 FDA device recall on record.
Top product codes for Carl Zeiss Suzhou Co., Ltd.
FDA recalls by Carl Zeiss Suzhou Co., Ltd.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Carl Zeiss Suzhou Co., Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.