FDA Device Intelligence
Home › PMT CORPORATION › Integra

Integra

PMT CORPORATION · Model 3611-663-2-EP · UDI-DI 00650551150435

LCJ Prescription
1
510(k) clearances
5,172
Adverse events (4 deaths)
21
Recalls
22
Facilities

Description

TE, IRREGULAR SHAPE, SMOOTH SURFACE, 2-STAGE, REMOTE EDGE PORT, 3.5X13.2CM, 290CC FILL, 5CM PROJECTION

Recalls

DateFirmReason
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18Mentor Texas, LP.Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-02B Braun Medical IncThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
2026-02-02B Braun Medical IncThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
2026-02-02B Braun Medical IncThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

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.