Ascension Orthopedics, Inc.
Ascension Orthopedics, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2024, with 1 FDA device recall on record.
Top product codes for Ascension Orthopedics, Inc.
FDA recalls by Ascension Orthopedics, Inc.
- Z-0794-2019 — Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number, MRH-350-04-WW
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ascension Orthopedics, Inc.
- K233674 — Freedom Wrist Arthroplasty System
- K233670 — Ascension Silicone MCP; Ascension Silicone PIP
- K121826 — INTEGRA PROXIMAL HUMERAL PLATE SYSTEM
- K110700 — ASCENSION ATLAS HUMERAL PLATING SYSTEM
- K102549 — THE ASCENSION MOVEMENT GREAT TOE SYSTEM TOTAL ARTHROPLASTY
- K100448 — ASCENSION MODULAR TOTAL SHOULDER SYSTEM
- K100502 — ASCENSION TOTAL PLATE SYSTEM
- K100925 — ASCENSION ANKLE FUSION NAIL SYSTEM
- K100176 — ASCENSION ANKLE FUSION PLATE SYSTEM
- K092047 — ASCENSION METAL GREAT TOE SYSTEM
- K092440 — ASCENSION CANNULATED SCREW SYSTEM
- K082231 — ASCENSION SILICONE PIP
- K080997 — ASCENSION PYROCARBON LUNATE
- K071064 — ASCENSION HUMERAL RESURFACING ARTHOPLASTY (HRA) SYSTEM TPS/HA
- K062861 — ASCENSION HUMERAL RESURFACING ARTHROPLASTY SYSTEM
- K061451 — ASCENSION, MODELS CMC-400,13,CMC-400-20,CMC-400-30,CMC-400-40
- K060560 — ASCENSION PYROSPHERE CMC/TMT
- K052137 — ASCENSION MUH
- K042690 — ASCENSION PYROSPHERE (PCS)
- K041451 — ASCENSION PYROHEMISPHERE, MODELS PHS-440-10, PHS-440-20, PHS-440-30, PHS-440-40, PHS-440-50
- K032686 — ASCENSION MODULAR RADIAL HEAD
- K022892 — ASCENSION SILLICONE MCP
Data sourced from openFDA. This site is unofficial and independent of the FDA.