Bionix Development Corp.
Bionix Development Corp. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2016.
Top product codes for Bionix Development Corp.
Recent clearances by Bionix Development Corp.
- K153270 — TruGuard Custom Tongue and Jaw Positioner
- K123411 — LITTLE ANGELS SWADDLING BLANKET
- K120335 — EMBRACE THERMOPLASTIC
- K100691 — OMNI V SBRT POSITIONING SYSTEM, MODEL RT-4500
- K100264 — T-FORM EXTREMITY IMMOBILIZER, MODEL RT-6060
- K050701 — THIGH AND FOOT POSITIONER, SUPRONE PLUS, MODEL RT-6010
- K040773 — PELVIS BELLYBOARD PLUS PATIENT POSITIONING SYSTEM
- K030051 — VERSABOARD, MODEL 7040
- K933613 — 3-WAY HEAD IMMOBILIZER; 3WAY DELUXE REUSABLE FRAME HEAD IMMOBILIZER
- K933614 — PITUITARY BOARD
- K905007 — STANDARD BREAST BOARDS; DELUXE BREAST BOARD
- K900370 — ONE/CIRC (CIRCUMCISION CLAMP)
Data sourced from openFDA. This site is unofficial and independent of the FDA.