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GuGwan Moxa Smokeless

Dong Bang Medical co.,Ltd. · Model DB 208A · UDI-DI 08800018916544

IMA
8
510(k) clearances
49
Adverse events
9
Recalls
87
Facilities

Recalls

DateFirmReason
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
2024-02-21Bruder Healthcare Company, LLCThermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.