Aesculap, Inc.
Aesculap, Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2026, with 40 FDA device recalls on record.
Clearances by Aesculap, Inc. — page 3
201–208 of 208- K922272 — YASARGIL ANEURYSM CLIPS
- K913730 — AESCULAP TITANIUM BONE PLATES
- K913765 — YASARGIL ANEURYSM CLIPS, MODIFICATION
- K913262 — AESCULAP SURGICAL ACCESSORIES
- K913415 — AESCULAP TITANIUM BONE SCREWS
- K904435 — VENTROFIL TENSION RELIEF SUTURE SET
- K904859 — MOTOR DRIVEN EXTIRPATION INSTRUMENTS
- K905143 — SKIN MARKER
Data sourced from openFDA. This site is unofficial and independent of the FDA.