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Conceive Plus

Model 8x4g · Sasmar Pharmaceuticals SPRL · DI 09337213008457

PEBLubricant, Personal, Gamete, Fertilization, And Embryo Compatible · Class II · 21 CFR 884.5300

UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

No dated reports to chart.

Regulatory clearances

  • K131355 SESE 2013-11-07 (k number procode)

Predicate lineage

K131355 — cites (transitively): K072741 (d1)

Lineage extracted from public 510(k) summary text (heuristic).

Manufacturer compliance record — Sasmar Pharmaceuticals SPRL

Nothing in the loaded window.