Pro Med Instruments GmbH
Pro Med Instruments GmbH holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2024, with 5 FDA device recalls on record.
Name variants for Pro Med Instruments GmbH
as filed with FDA- Pro Med Instruments GmbH
- Pro-Med Instruments GmbH
Top product codes for Pro Med Instruments GmbH
FDA recalls by Pro Med Instruments GmbH
- Z-1860-2025 — DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
- Z-2970-2018 — DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
- Z-2971-2018 — DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
- Z-2972-2018 — DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
- Z-0193-2018 — pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), STERILE R, Rx ONLY The DORO(R) Skull Pins are inserted into the receptacles of the skull clamp and fixate the head during surgery.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Pro Med Instruments GmbH
- K241883 — DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00) +4 more
- K240319 — DORO LUCENT Skull Clamp (1101.001); DORO LUCENT Skull Clamp Pediatric Set (1101.040)
- K203505 — DORO QR3 Headrest System (Aluminum)
- K193438 — DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile Disposable Skull Pins (Titanium)
- K191740 — DORO LUCENT® iXI and iMRI Headrest System
- K191979 — DORO QR3 XTom Headholder System
- K063494 — DORO RADIOLUCENT HEADREST SYSTEM ( ALSO MRI-COMPATIBLE) AND COMPONENTS
- K070997 — DORO NON-STICK BIPOLAR FORCEPS, MODEL 5001-XX TO 5012-XX, DORO BIPOLAR REUSABLE CABLES, MODEL 5015-XX
- K032331 — DORO RADIOLUCENT HEADREST SYSTEM AND HORSESHOE HEADRESTS,AND NON-RADIOLUCENT J-ARM RETRACTOR SYSTEM (ALUMINUM ALLOY)
- K001808 — DORO HEADREST SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.