Metalor Dental USA Corp.
Metalor Dental USA Corp. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2001.
Top product codes for Metalor Dental USA Corp.
Recent clearances by Metalor Dental USA Corp.
- K003387 — AUROFILM NP
- K993475 — AUROFLUID M, ALLOY NO. 5315
- K993505 — V-DELTA SPECIAL, ALLOY NO. 5154
- K993506 — PAGALINOR 4 , ALLOY NO. 5440
- K993507 — V-SUPRAGOLD, ALLOY NO. 5024
- K993508 — V-SUPRA PLUS, ALLOY NO. 5025
- K993474 — DELTAPAL, ALLOY NO. 5161
- K982606 — AUROFLUID CPF
- K973372 — AUROFILM 2000
- K972683 — V-DELTA 450
- K970044 — AUROFLUID 22
- K970045 — SOLARO 33
- K954702 — IMPLANTALOY
- K951271 — VS11 SF
- K952499 — VS1 PLUS
- K952122 — V-GNATHOS PLUS
- K933563 — VS 1A
- K924155 — SURA SNAP
- K925973 — VS1 GPF, VACU PF
- K925974 — CASTING GOLD,CERAMIC,GOLD WIRE,ALLOY PRECISION ATT
- K924292 — CERAPALL 6 -- MODIFIED
- K921794 — CERADELTA 2
- K915111 — PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD
- K914627 — PLATINUM FOIL PLATINUM MILING WAFER
- K912435 — DENTAL CONNECTOR PRECISION ATTACHMENT
- K912720 — ENDO-CORE
- K912721 — AUROFILM MP
- K911669 — CERAPALL 6
- K911674 — CERAPLUS
- K912302 — VACU 2
- K912305 — STANDARD S3
- K912307 — STANDARD S31
- K912308 — STANDARD S32
- K912313 — SOLCHROM-PAL
- K911671 — CERADELTA
- K911545 — V-DELTA
- K912314 — 800 SOLDER
- K912315 — V-DELTA S1
- K912567 — CONICAST, INTRACAST, OMECAST
- K911668 — CERAPALL 2
- K911675 — PAGALIN 2
- K911677 — SELECTOR 3
- K912297 — VS1G
- K912298 — VS1
- K912299 — VS1B
- K912300 — VS11
- K912303 — STANDARD S1
- K912304 — STANDARD S2
- K912306 — STANDARD S4
- K912309 — STANDARD S33
- K911670 — CERAPALL
- K911546 — INLAY 90
- K911530 — V-GNATHOS
- K911531 — V-SUPERGOLD
- K911532 — V-SUPER
- K911533 — V92
- K911534 — V44
- K911535 — V-CLASSIC
- K911536 — V-DELTABOND
- K911537 — V-DELTA, SF
- K911538 — AUROFLUID 2
- K911539 — AUROFLUID 3
- K911540 — PROTH-AURO 22
- K911541 — PONTOR 4 CF
- K911542 — PONTOR 2
- K911543 — SOLARO 3
- K911544 — SOLARO 4
Data sourced from openFDA. This site is unofficial and independent of the FDA.