FDA Device Intelligence
Home › Peter Brasseler Holdings, LLC › Brasseler USA

Brasseler USA

Peter Brasseler Holdings, LLC · Model 5013514U0 · UDI-DI 00887919576129

ELR Prescription
10
510(k) clearances
131
Adverse events
2
Recalls
98
Facilities

Description

ESP9006 SEQ POST .90MM .06 TAPE

Recalls

DateFirmReason
2018-08-21Coltene Whaledent IncParaPost Plus Titanium Posts contain stainless steel post that are a size 4
2009-03-20Dentsply Worldwide HeadqrtThe product is manufactured with a left-hand thread instead of a right hand thread. This error could cause tooth breakage if the posts were removed without knowing that the thread

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.