Embody, Inc.

FDA Device Registration & Listing · Norfolk, VA, US · Registration 3015543569

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015543569
FEI Number
3015543569
Entity Name
Embody, Inc.
City/State/Country
Norfolk, VA, US
Establishment Address
4211 Monarch Way, Suite 500, Norfolk, VA 23508, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Embody, Inc. (Owner Number: 10079091)
Owner / Operator Contact Address
4211 Monarch Way, Suite 500, Norfolk, VA 23508, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K252647
PMA Number
N/A

All Registered Proprietary Names

Tapestry Biointegrative Implant ActivBraid Tapestry RC Biointegrative Implant System Dual Anchor Inserter with Bioabsorbable Anchors Tapestry Biointegrative Implant

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon General, Plastic Surgery Class 2 878.3300 2025-12-17
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2023-07-12
OJH Orthopedic Tray General, Plastic Surgery Class 1 878.4800 2025-01-09
MAI Fastener, Fixation, Biodegradable, Soft Tissue Orthopedic Class 2 888.3030 2022-04-21
OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon General, Plastic Surgery Class 2 878.3300 2025-09-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Embody, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K072322 Smith & Nephew, Inc. ULTRA FAST-FIX AND ULTRA FAST-FIX AB MENISCAL REPAIR SYSTEMS 2007-09-18
K203334 Acuitive Technologies, Inc. The Citrefix Knotless Suture Anchor 2021-02-05
K243467 Osteonic Co., Ltd. Fix2Lock (Biocomposite medial, Biocomposite lateral, Biocombi Self Punching) 2024-12-03
K213415 OSSIO , Ltd. OSSIOfiber Suture Anchor 2022-03-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015543569. Last updated year: 2026. Please use registration number 3015543569 when referencing this establishment in official correspondence.
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