Opus Medical, Inc.
FDA 510(k) medical device clearances.
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.