ClearanceBrief
Company · US

Embody, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2025. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OWYMesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon4
GATSuture, Nonabsorbable, Synthetic, Polyethylene1
MAIFastener, Fixation, Biodegradable, Soft Tissue1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 19, 2025K252647Tapestry Biointegrative Implant
Embody, Inc.
OWY
Jun 2, 2023K223822ACTIVBRAID™
Embody, Inc.
GAT
May 23, 2022K220867Tapestry Biointegrative Implant
Embody, Inc.
OWY
Apr 8, 2022K213958Bioabsorbable Anchor
Embody, Inc.
MAI
Nov 2, 2021K212306Tapestry Biointegrative Implant
Embody, Inc.
OWY
Oct 19, 2020K201572TAPESTRY Biointegrative Implant
Embody, Inc.
OWY

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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