BHI Implants

FDA Device Registration & Listing · Afula Northern, IL · Registration 3010393542

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010393542
FEI Number
3010393542
Entity Name
BHI Implants
City/State/Country
Afula Northern, IL
Establishment Address
Hamal 2, Afula Northern 1857107, IL
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
BHI Implant l Ltd. (Owner Number: 10044723)
Owner / Operator Contact Address
2 Hamal Street, POB 1063,Industrial Park, Afula, IL-Z 1857107, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RS-OPD425 RS-OPD550 RS-OPD450 RS-OPD300 RS-OPD500 RS-OPD250 BH-1220 BH-HD2S BH-2100 BH-HD1S BH-MT20 BH-MK2L BH-1120 BH-2000 BH-1MKS BH-DE10 BH-1110 BH-HD1H BH-2200 BH-MK2S BH-TD20 BH-TD37 BH-TD47 BH-HD2L BH-HD1L BH-TD27 BH-TD42 BH-TD32 BH-TD400L16 BH-TD300L16 BH-TD350L16 BH-TD580L16 BH-2010 CD 5x6 CD 3.75x4.20 BH-STT2 BH-SSD1 BH-STT1 GIH-SK01 BH-1MKL BH-TD280L16 BH-TD320L16 BH-TD450L16 TDC330L16 BH-2300 TD320L16 BH-TD520L16 BH-CTTS TD380L16 BH-TD380L16 PD200L16 BH-PD200L16 BH-TD470L16 TD580L16 MDL 1.90 TD500L16 TD300L16 BH-TD420L16 BH-TD370L16 BH-PA01 BH-CTTL BH-PA02 BH-CL10 BH-PKI1 BH-MD20 BH-PCBP BH-HD2H BH-TD480L16 BH-CODR MDI 1.90 BH-TD365L16 BH-112W BH-OTTS BH-CTTLS TDC280L16 TD365L16 TD550L16 TD280L16 BH-OTTL TD420L16 TD520L16 TD410L16 TD400L16 TD350L16 TD480L16 BH-BTCP BH-MUOTTR BH-BARS BH-TBH001 BH-MUANG BH-BARL BH-MUTS BH-IB92 BH-MUTRSC BH-TBG330 BH-MUHLDR BH-IB81 BH-TBZ100 BH-MUPS TDE BH-TBC100 BH-SMUDRVR BH-TBB001 BH-TBD375C BH-TBD330C GIH-MUTS BH-IB91 BH-TBG375 BH-TBD200 GIH-OTTL GIH-CTTL GIH-MUANG GIH-MUOTTR BH-MUTB GIH-MUANG5 BH-MUSP GIH-MUDA GIH-HD1H BH-MUDA GIH-1220 BH-SP4507 GIH-2300 EZ-MUTSSP BH-TBD180 T4213-L GIH-MUPS MUSB005DG BH-IMPDIAN BH-SP4509 GIH-SMUDRVR MUP001 GIH-HD2H MUT004-C A5024 RMUASB07 RSBIMP07 A3824 COCR05-R GIH-IMPDIAN BH-BALLAN T4209-L MUA005DG T4213-S GIH-SP4509 RMUATRF SBODP9 LOCS10 SCA03 SCA02 RMUASB13 LOCS30 RMUASB10-1.6 BMC05 RMUASB13-1.72 IT-BS2x19 LOCM10 RSD242 SBODP7 IT-BS2x13 GIH-RMUDA DAR24 BH-SP.MUANG IT-LP10 MUT004-O RMUASB13-1.6 SCA04 SCA01 RSBIMP09 SCP001 RMUASLV T4209-S BSC01 RDAIMP MUA005 ZO-BALL COCR05-H RMUASB10 PAN105 RS-OPD475 MUT002 PAH105 LOCS20 RMUASB10-1.72 RMUADA RS-OPD525 RS-OPD325 RS-OPD225 RMUASB07-1.72 RS-OPD275 IT-BSSL4 RS-OPDKIT RS-OPD350 RS-OPD375 RMUASB07-1.6 RS-OPD400

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NDP Accessories, Implant, Dental, Endosseous Dental Class 1 872.3980 2013-07-18

Official Correspondent

Asaf Feuerstein

US Agent Details

Arik Vrobel Email: AVROBEL@YAHOO.COM Phone: (714) 2306122

Related Public Records

Same Entity

BHI Implant l Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment SP, Cat. No. 30-70101 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0014-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment NP, Cat. No. 30-70102 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0015-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0016-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment SU, Cat. No. 30-70104 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0017-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment PCA, Cat. No. 30-70105 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010393542. Last updated year: 2026. Please use registration number 3010393542 when referencing this establishment in official correspondence.
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