Coalign Innovations, Inc.

Coalign Innovations, Inc. holds 9 FDA 510(k) medical device clearances, first cleared 2011, most recent 2013.

Top product codes for Coalign Innovations, Inc.

MAX — Orthopedic9 devices

Recent clearances by Coalign Innovations, Inc.

K132505 — ACCULIF TL AND PL CAGECode MAX·2013-09-12
K131443 — COALIGN INNOVATIONS ACCULIF XL IBF CAGECode MAX·2013-06-19
K130194 — ACCULIF XL CAGECode MAX·2013-04-03
K123281 — ACCULIF TL-PEEK CAGECode MAX·2013-01-23
K123752 — ACCULIF TL AND PL CAGECode MAX·2013-01-14
K121683 — ACCULIF TL CAGECode MAX·2012-07-05
K113465 — ACCULIF TL CAGECode MAX·2011-12-12
K112095 — ACCULIF TL-PEEK IBF CAGECode MAX·2011-12-01
K110270 — ACCULIF CAGECode MAX·2011-04-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.