Wilde-USA, Inc.

16 FDA 510(k) medical device clearances.

Top product codes for Wilde-USA, Inc.

EBI — Dental 4 devices
EBF — Dental 2 devices
EJJ — Dental 2 devices
EBZ — Dental 1 device
EIH — Dental 1 device
EJH — Dental 1 device
ELM — Dental 1 device
ELW — Dental 1 device
EMI — Dental 1 device
FMC — General Hospital 1 device

Recent clearances by Wilde-USA, Inc.

K913582 — COMPATIT R ELM · 1993-06-24
K915653 — KERAMAIL EIH · 1993-04-08
K913581 — WILDE ADHESIVE BONDING SYSTEM KLE · 1993-02-26
K923472 — COMPACOLOR EBF · 1992-10-13
K920649 — COMPASEP FMC · 1992-07-23
K913089 — WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS EBF · 1992-04-21
K915250 — WIL-PDS & WIL-PDI CASTING ALLOYS EJH · 1992-04-21
K912990 — CONVERBASE EBI · 1992-03-25
K920557 — WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX EBI · 1992-03-20
K915654 — KERALLOY-D CAPS EJJ · 1992-03-02
K912993 — WILDE DENTURE RESINS EBI · 1992-02-03
K912994 — COMPALUX STROBOSCOPIC LIGHT POLYMERIZATION DEVICE EBZ · 1991-12-23
K912991 — WILDE AUXILIARIES EBI · 1991-12-19
K912992 — KERALLOY NON-GAMMA 2 AMALGAM EJJ · 1991-11-13
K913583 — CONVERSIL FL AND CONVERSIL P ELW · 1991-11-13
K912989 — PLANUSTAR AND DENS NOBILIS DENTURE TEETH EMI · 1991-08-16

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