Anulex Technologies, Inc.
Anulex Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2012.
Top product codes for Anulex Technologies, Inc.
Recent clearances by Anulex Technologies, Inc.
- K121354 — MICRO/MINI N-PK(F) BONE ANCHOR
- K121356 — MICRO/MINI N-PK(H) BONE ANCHOR
- K113805 — FIXATE TISSUE BAND
- K113400 — FIXATE TISSUE BAND
- K112849 — FIXATE TISSUE BAND
- K111462 — FIXATE TISSUE BAND
- K100572 — VERSACLOSE, MODEL VC-200-01
- K091432 — XCLOSE TISSUE REPAIR SYSTEM, MODEL XC-200-01
- K082729 — RIMCLOSE BONE ANCHOR
- K062307 — XCLOSE TISSUE REPAIR SYSTEM, MODEL SRS
- K061386 — ANCHOR BAND SUTURING SYSTEM, MODEL SR-AB
- K050969 — INCLOSE SURGICAL MESH SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.