# Embody Post-Market Clinical Follow-Up Study

> **NCT05735119** · — · ENROLLING_BY_INVITATION · sponsor: **Zimmer Biomet** · enrollment: 100 (estimated)

## Conditions studied

- Tendon Injuries- Subscapularis

## Interventions

- **DEVICE:** Tapestry Biointegrative Implant

## Key facts

- **NCT ID:** NCT05735119
- **Lead sponsor:** Zimmer Biomet
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2022-11-09
- **Primary completion:** 2026-09
- **Final completion:** 2028-03
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2026-02-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05735119

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05735119, "Embody Post-Market Clinical Follow-Up Study". Retrieved via AI Analytics 2026-06-16 from https://api.ai-analytics.org/clinical/NCT05735119. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
