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Imz, GmbH

Potomac, MD, US

Imz, GmbH appears in FDA device records in Potomac, MD. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
12
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 12 510(k) clearances for Imz, GmbH between 1995 and 1997. The busiest year on record is 1995, with 8. The most recent is 1997, with 4.

Clearances by year, as a table
510(k) clearance decisions for Imz, GmbH, by decision year
YearClearances
19958
19974
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K963520IMZ TWIN PLUS SCREWDZESubstantially Equivalent
K963521IMZ TWIN PLUS - CYLINDERDZESubstantially Equivalent
K963522IMZ 2000 INTERLOCK 12/3 - SCREWDZESubstantially Equivalent
K963495IMZ 2000 INTERLOCK 12/3 - CYLINDER DENTAL IMPLANT SYSTEMDZESubstantially Equivalent
K951611IMZ - DENTAL IMPLANT SINGLE TOOTH ATTACHMENTDZESubstantially Equivalent
K951609IMZ - DENTAL IMPLANT SURGICAL TRAYDZESubstantially Equivalent
K951618IMZ - DENTAL IMPLANT O-RING ATTACHMENTDZESubstantially Equivalent
K951617IMZ - DENTAL IMPLANT CASTABLE CSR ATTACHMENTDZESubstantially Equivalent
K951615IMZ - DENTAL IMPLANT COMPONENTSDZESubstantially Equivalent
K951614IMZ - DENTAL IMPLANTDZESubstantially Equivalent
K951612IMZ - DENTAL IMPLANT COMPONENTSDZESubstantially Equivalent
K951610IMZ - DENTAL IMPLANTDZESubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain