Biotronik, Inc.: PMA supplement approved for Ilivia Neo 7 VR-T DX 429530; Intica Neo 7 VR-T DX 429559; Intica Neo 5 VR-T DX 429569

Biotronik, Inc. (Lake Oswego, Oregon): PMA supplement approved for Ilivia Neo 7 VR-T DX 429530; Intica Neo 7 VR-T DX 429559; Intica Neo 5 VR-T DX 429569. Dated 41 days ago, it serves as a historical benchmark. Score 30/100. As of 2026-11-04, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)

Free preview: all 8 published fields of this record are shown below. Locked: 19 related OR FdaApprovalPulse records and the 4-column CSV export.

FieldValue
SponsorBiotronik, Inc.
ProductIlivia Neo 7 VR-T DX 429530; Intica Neo 7 VR-T DX 429559; Intica Neo 5 VR-T DX 429569
Generic / ingredientImplantable cardioverter defibrillator (non-CRT)
ApprovalPMA supplement (device change)
ApplicationP980023 S140
Decided2026-09-25
Panel / classCardiovascular
Sponsor locationLake Oswego, OR
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  • Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
  • Record date: 2026-09-25
  • Data refreshed: 2026-11-04
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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 06:06:18 GMT

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Peer benchmark and outreach value: Biotronik, Inc. and 20 Oregon peers

  • Oregon FdaApprovalPulse records like this one: 20
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Oregon peer: $4,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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30 / 100 Score

    What is the FdaApprovalPulse record for Biotronik, Inc. in Lake Oswego, Oregon?

    The FDA approved Ilivia Neo 7 VR-T DX 429530; Intica Neo 7 VR-T DX 429559; Intica Neo 5 VR-T DX 429569 (P980023 S140) for Biotronik, Inc. on 2026-09-25: PMA supplement (device change).

    How does Biotronik, Inc. compare to other Oregon FdaApprovalPulse records?

    It is 41 days old, still within a typical 45-day follow-up window. Its Score of 30/100 is modest; treat it as background rather than a priority.

    Biotronik, Inc. vs. top 3 peers

    OrganizationLocationRecord date
    Biotronik, Inc.Lake Oswego, OR2026-09-25
    Instylla, Inc.Bedford, MA2026-10-23
    Ventana Medical Systems, Inc. (Roche Tissue Diagnostics)Tucson, AZ2026-10-23
    Cerenovus, Inc.Miami, FL2026-10-23

    Related records

    FdaApprovalPulse: PMA supplement (device change) FdaApprovalPulse: records in Oregon

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    ✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

    From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.

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