Product code LGF— Orthopedic
DELTA-LITE CASTING RESIN
- Classification name
- Component, Cast
- Device class
- Class 1
- Regulation
- 21 CFR 888.5940
- Advisory panel
- Orthopedic
- Total cleared
- 31
- First cleared
- Most recent
Market context for product code LGF
FDA has cleared devices under product code LGF between 1978 and 2005, filed by 22 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
last 15 years- 2005
- 1997
- 1996
- 1994
- 1993
- 1991
- 1990
- 1988
- 1987
- 1986
- 1985
- 1984
- 1983
- 1982
- 1981
Top applicants under product code LGF
Recent clearances under product code LGF
- K043526 — SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATIC
- K973417 — CLINITEX STOCKINETTE
- K973420 — CLINITEX CAST PADDING
- K955320 — PROTEC COTTON PADDING BANDAGE
- K932507 — QUICK-CAST IMMOBILIZER
- K931672 — CARAPACE STERILE CAST PADDING
- K910274 — ARTIFLEX(TM)
- K903946 — COOL CAST(R)
- K896634 — CARAGLAS XTRA SYNTHETIC CASTING TAPE
- K883294 — SYNTHETIC CAST TAPE
- K874880 — COLORED CASTING TAPE CARAGLAS(TM GREEN
- K873717 — CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135
- K873718 — CHILD WALKING HEEL PRODUCT NO. 4183-132
- K873722 — PEDESTAL WALKING HEEL PRODUCT NO. 4183-133
- K870404 — COLORED CASTING TAPE (RED AND BLUE)
- K864092 — OEC DESIGN ORTHOPEDIC CAST HEEL
- K861073 — AMERICAN ORTHOPAEDIC VACUUM 0295-250
- K861074 — AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-200
- K861075 — AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-202
- K854554 — DELTA-LITE CASTING RESIN
- K854341 — DELTA-LITE CASTING RESIN
- K843780 — VENT-A-CAST
- K840617 — MASTERFOOT CAST HEEL
- K833084 — MASTERHINGE
- K823819 — CAST TOE COVER
- K823394 — WALKING HEEL
- K822059 — SHOW'RBAG
- K812904 — STERILE ORTHOPEDIC STOCKINETTE
- K810110 — COBBLER'S CHIP SPLINTS
- K803141 — CONPHAR CAST HEELS
- K780283 — INSERTER, PLUG, BONE, LIDGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.