3M Company
3M Company holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2025, with 2 FDA device recalls on record.
Clearances by 3M Company — page 4
301–331 of 331- K802751 — P-10 POSTERIOR FILLING MATERIAL
- K802242 — 3M HI-STRENGTH MED. TAPE #1534
- K801057 — 3M STEAM STERILIZATION INDICATOR
- K801041 — 3M R.F. CURRENT SUPPRESSOR
- K800487 — 3M TITANIUM ALLOY TOTAL HIP SYSTEM 32MM
- K800758 — TENZCARE DUAL-CHANNEL STIMULATOR
- K800535 — 3M DISPOSABLE SKIN STAPLER
- K800485 — VINYL POLYSILOXANE IMPRESSION MATERIAL
- K792050 — 3M SMALL VOLUME INFUSTION (SVI) SYSTEM
- K791789 — 3M MICROBIAL PROFILE SYSTEM GRAM
- K791894 — 3M BRAND TOTAL LEG COMPRESSION TLC SYS.
- K792181 — 3M HS 22 FEMORAL COMPONENT
- K791823 — 3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM
- K791960 — ROTH-KENNEDY PASSER
- K791056 — 3M CEMENT REMOVER
- K791176 — 3M COLD/HOT WATER BAG AND WRAP
- K791094 — 3M ORTHOPEDIC CASTING TAPE
- K791057 — CAST BRACE COMPONENTS
- K790850 — T.E.N.S.* SINGLE-USE ELECTRODE
- K790654 — CLOSED WOUND VACUUM DRAINAGE SYSTEM
- K790307 — FLEXIBLE REAMER, GUIDE WIRE SYSTEM
- K781098 — BRUSH, APPLICATOR
- K781097 — INOCULUM STDIZING SYS., INOCUPAC
- K780088 — HYMIDIFIER
- K780028 — ORTHODONTIC. PLASTIC BRACKET PRIMER
- K771511 — TOTAL KNEE PROSTHESIS-NONCONSTRAINED
- K771908 — ISO-SHIELD SALIVA ABSORBERS
- K771547 — PETITES BETWEEN-PERIOD PROTECTORS
- K771653 — ELECTRONIC STETHOSCOPE
- K771253 — HEMOX-ANALYZER
- K760611 — 3M BRAND ANESTHESIA FILTER,#3110
Data sourced from openFDA. This site is unofficial and independent of the FDA.