Opus Medical, Inc.
Opus Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2004.
Top product codes for Opus Medical, Inc.
Recent clearances by Opus Medical, Inc.
- K042584 — OPUS MINIMAGNUM ANCHOR WITH INSERTER
- K042914 — OPUS MAGNUM KNOTLESS ANCHOR WITH INSERTER HANDLE
- K042031 — OPUS SPEEDSTITCH SUTURE DEVICE
- K041440 — OPUS MAGNUM ANCHOR WITH INSERTER
- K033317 — SMARTSTITCH M-CONNECTOR, MODEL OM-8700; NEEDLE CASSETTE, OM-8750; AUTOCUFF SYSTEM INSTRUMENT SET, OM-9070
- K030170 — REUSABLE SMARTSTITCH SUTURE DEVICE, MODELS OM-8007, OM-8500
- K031083 — OPUS MAGNUM IMPLANT SYSTEM, MODEL OM-1500
- K030235 — F1 DIODE LASER SYSTEM
- K023843 — SMARTSTITCH M-CONNECTOR, MODEL OM-8005; SMARTSTITCH ACTUATION HANDLE, MODEL OM-8500; AND SMARTSTITCH SUTURE CARTRIDGE
- K022229 — SMARTSTITCH SUTURE DEVICE, MODEL OM-8500
- K020172 — OPUS MAGNUM ANCHOR & INSTRUMENT SET
- K012125 — OPUS MAGNUM ANCHOR & INSERTER
- K004021 — F1 DIODE LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.