FDA Device Intelligence
Home › PDT, INC. › PDT, Inc.

PDT, Inc.

PDT, INC. · Model R979 DDS Exam Kit · UDI-DI 00813677024459

EAXEJBEKBEIXFSMEJY
10
510(k) clearances
47
Adverse events
1
Recalls
371
Facilities

Description

Kit Includes: T005A-F FlipTop™ Cassette 'A' - Fixed Rack 5 R245 Mirror Handle (Cone-Socket) T050 #5 Front Surface Mirror, Cone-Socket, (15/16') R166 Explorer 5 R215 Probe WRS ACE™-UNC12 T040 Tweezers COLLEGE

Recalls

DateFirmReason
2021-03-23Sunstar Americas, Inc.Product may be contaminated with Burkholderia contaminans.

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.